Process for preparing alpha-substituted acrylates

Abstract

The present disclosure relates to a process for preparing an alpha-substituted acrylate, the process comprising: a) combining starting materials comprising an alpha-(halomethyl)acrylate and an organoaluminum compound, thereby forming a product comprising the alpha-substituted acrylate.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of priority to U.S. Application No. 62 / 954,956, filed December 30, 2019, which is incorporated by reference in its entirety. [Background technology]

[0002] Alpha-substituted acrylates, such as alpha-(alkyl)acrylates or alpha-(polymeryl)acrylates, are important intermediates for preparing useful polymeric materials. Synthetic routes for the preparation of alpha-substituted acrylates and bisacrylates from organozinc reagents are known in the art. However, such routes employ transmetallation of organozinc compounds to organocopper compounds, and the direct reaction of organoaluminum compounds with halomethylacrylates is not known. The present disclosure addresses such a need by demonstrating the direct reaction of organoaluminum compounds with alpha-(halomethyl)acrylates to synthesize alpha-(alkyl) and alpha-(polymeryl)acrylates. Summary of the Invention

[0003] The present disclosure relates to a process for preparing an alpha-substituted acrylate, the process comprising: a) combining starting materials including an alpha-(halomethyl)acrylate and an organoaluminum compound; thereby forming a product comprising an alpha-substituted acrylate. [Brief description of the drawings]

[0004] [Figure 1A] 1 provides the NMR spectrum of Example 1. [Figure 1B] 1 provides the NMR spectrum of Example 1. [Figure 2A] 1 provides the NMR spectrum of Example 2. [Figure 2B]1 provides the NMR spectrum of Example 2. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0005] definition All references herein to the Periodic Table of the Elements shall refer to the Periodic Table of the Elements published and copyrighted in 2003 by CRC Press, Inc., and any references to a Group(s) shall be to the Group(s) reflected in that Periodic Table of the Elements using the IUPAC system for numbering the Groups.

[0006] Unless expressly stated, implied by context, or customary in the art to the contrary, all parts and percentages are by weight.

[0007] For purposes of United States patent practice, the contents of any patents, patent applications, or publications referenced herein are hereby incorporated by reference in their entirety (or their equivalent U.S. versions are so incorporated by reference), particularly with respect to the present disclosure of synthetic techniques, definitions (to the extent not inconsistent with any definitions provided herein), and general knowledge in the art.

[0008] Numeric ranges disclosed herein include all values, inclusive, between the lower and upper limits. Ranges including explicit values ​​(e.g., 1, or 2, or 3-5, or 6, or 7) also include any subranges between any two explicit values ​​(e.g., 1-2, 2-6, 5-7, 3-7, 5-6, etc.). Numeric ranges disclosed herein further include fractions between any two explicit values.

[0009] The terms "comprising," "including," "having," and their derivatives are not intended to exclude the presence of any additional component, step, or procedure, whether or not it is specifically disclosed. In contrast, the term "consisting essentially of" excludes from the scope of any succeeding recitation any other component, step, or procedure, excepting those that are not essential to operability. The term "consisting of" excludes any component, step, or procedure not specifically delineated or listed. The term "or," unless expressly stated otherwise, refers to the listed items individually as well as in any combination.

[0010] As used herein, the terms "hydrocarbyl", "hydrocarbyl group", and the like refer to compounds composed entirely of hydrogen and carbon, including aliphatic, aromatic, acyclic, cyclic, polycyclic, branched, unbranched, saturated, and unsaturated compounds. The terms "hydrocarbyl", "hydrocarbyl group", "alkyl", "alkyl group", "aryl", "aryl group", and the like are intended to include all possible isomers, including all structural or stereoisomers.

[0011] The term "cyclic" refers to a series of atoms in a polymer or compound that includes one or more rings. Thus, the term "cyclic hydrocarbyl group" refers to a hydrocarbyl group that contains one or more rings. As used herein, a "cyclic hydrocarbyl group" may contain acyclic (linear or branched) portions in addition to the one or more rings.

[0012] "Transmetalation" or "transmetallation" refers to an organometallic reaction involving the transfer of a ligand from one metal to another.

[0013] The term "catalyst" is used interchangeably with terms such as "procatalyst," "precatalyst," "catalyst precursor," "transition metal catalyst," "transition metal catalyst precursor," "polymerization catalyst," "polymerization catalyst precursor," "transition metal complex," "transition metal compound," "metal complex," "metal compound," "complex," "metal-ligand complex," and the like.

[0014] "Cocatalyst" refers to a compound capable of activating a particular procatalyst to form an active catalyst capable of polymerizing unsaturated monomers. The term "cocatalyst" is used interchangeably with terms such as "activator."

[0015] The terms "active catalyst", "active catalyst composition" and the like refer to a transition metal compound capable of polymerizing unsaturated monomers with or without a cocatalyst. An active catalyst may be a "procatalyst" that becomes active for polymerizing unsaturated monomers without a cocatalyst. Alternatively, an active catalyst may be a "procatalyst" that becomes active in combination with a cocatalyst for polymerizing unsaturated monomers.

[0016] The term "polymer" refers to a material prepared by reacting (i.e., polymerizing) a set of monomers, which may be a homogeneous (i.e., only one type) set of monomers or a heterogeneous (i.e., two or more types) set of monomers. As used herein, the term polymer includes the term "homopolymer," which refers to a polymer prepared from a homogeneous set of monomers, and the term "interpolymer," as defined below.

[0017] The term "interpolymer" refers to a polymer prepared by polymerization of at least two different types of monomers. The term includes both "copolymers", i.e., polymers prepared from two different types of monomers, and polymers prepared from three or more different types of monomers, e.g., terpolymers, tetrapolymers, etc. The term also encompasses all forms of interpolymers, such as random, block, uniform, heterogeneous, etc.

[0018] "Polyolefin" is a polymer made from the polymerization of olefins as monomers, where the olefin monomers are linear, branched, or cyclic compounds of carbon and hydrogen with at least one double bond. Thus, as used herein, the term "polyolefin" includes and encompasses the terms "ethylene-based polymer", "propylene-based polymer", "ethylene homopolymer", "propylene homopolymer", "ethylene / alpha-olefin interpolymer", "ethylene / alpha-olefin copolymer", "ethylene / alpha-olefin multi-block interpolymer", "block composite", "particular block composite", "crystalline block composite", "propylene / alpha-olefin interpolymer", and "propylene / alpha-olefin copolymer".

[0019] An "ethylene-based polymer" is a polymer that contains a majority amount of polymerized ethylene, based on the weight of the polymer, and may optionally further contain polymerized units of at least one comonomer. An "ethylene-based interpolymer" is an interpolymer that contains a majority amount of ethylene in polymerized form, based on the weight of the interpolymer, and further contains polymerized units of at least one comonomer. An "ethylene homopolymer" is a polymer that contains repeat units derived from ethylene, but does not exclude residual amounts of other components.

[0020] As used herein, the term "ethylene / alpha-olefin interpolymer" refers to a polymer that comprises, in polymerized form, a majority weight percent of ethylene (based on the weight of the interpolymer) and at least one comonomer that is an alpha-olefin. Ethylene / alpha-olefin interpolymers can be random or block interpolymers. The terms "ethylene / alpha-olefin copolymer" and "ethylene / alpha-olefin multi-block interpolymer" are encompassed by the term "ethylene / alpha-olefin interpolymer."

[0021] As used herein, the term "ethylene / alpha-olefin copolymer" refers to a copolymer that contains, in polymerized form, a majority weight percent of ethylene (based on the weight of the copolymer) and a comonomer that is an alpha-olefin, where ethylene and the alpha-olefin are the only two monomer types. Ethylene / alpha-olefin copolymers can be random or block copolymers.

[0022] As used herein, "ethylene / alpha-olefin multi-block interpolymer" or "olefin block copolymer" refers to an interpolymer comprising ethylene and one or more copolymerizable alpha-olefin comonomers in polymerized form, characterized by a plurality of blocks or segments of two or more (preferably three or more) polymerized monomer units, the blocks or segments differing in chemical or physical properties. Specifically, the term refers to a polymer comprising two or more (preferably three or more) chemically distinct regions or segments (referred to as "blocks") linked in a linear fashion, i.e., chemically distinct units that are linked end-to-end (covalently bonded) with respect to polymerized functional groups, rather than in a pendant or grafted fashion. The blocks differ in the amount or type of comonomer incorporated therein, density, amount of crystallinity, type of crystallinity (e.g., polyethylene vs. polypropylene), size of crystals resulting from polymers of such composition, type or degree of stereoregularity (isotactic or syndiotactic), regioregularity or regioirregularity, amount of branching, including long chain branching or hyperbranching, uniformity, and / or any other chemical or physical property. The block copolymers are characterized by unique distributions of both polymer polydispersity (PDI or Mw / Mn) and block length distribution, for example, based on the use of a shuttling agent in combination with a catalyst system.Non-limiting examples of the olefin block copolymers of the present disclosure and the process for preparing same are disclosed in U.S. Patent Nos. 7,858,706 (B2), 8,198,374 (B2), 8,318,864 (B2), 8,609,779 (B2), 8,710,143 (B2), 8,785,551 (B2), and 9,243,090 (B2), all of which are incorporated herein by reference in their entirety.

[0023] The term "block composite" (BC) refers to a polymer comprising three polymer components: (i) an ethylene-based polymer (EP) (soft copolymer) having an ethylene content of 10 mol% to 90 mol%, based on the total moles of polymerized monomer units in the ethylene-based polymer (EP); (ii) an alpha-olefin-based polymer (AOP) (hard copolymer) having an alpha-olefin content of more than 90 mol%, based on the total moles of polymerized monomer units in the alpha-olefin-based polymer (AOP); and (iii) a block copolymer (e-block copolymer) having an ethylene block (EB) and an alpha-olefin block (AOB), where the ethylene block of the block copolymer has the same composition as the EP of component (i) of the block composite, and the alpha-olefin block of the block copolymer has the same composition as the AOP of component (ii) of the block composite. In addition, the compositional distribution between the amount of EP and the amount of AOP in the block composite will be essentially the same as the compositional distribution between the corresponding blocks in the block copolymer. Non-limiting examples of block composites of the present disclosure, and processes for preparing the same, are disclosed in US Pat. Nos. 8,686,087 and 8,716,400, which are incorporated herein by reference in their entireties.

[0024] The term "specified block composite" (SBC) refers to a polymer that includes three polymer components: (i) an ethylene-based polymer (EP) (soft copolymer) having an ethylene content of 78 mol% to 90 mol%, based on the total moles of polymerized monomer units in the ethylene-based polymer (EP); (ii) an alpha-olefin-based polymer (AOP) (hard copolymer) having an alpha-olefin content of 61 mol% to 90 mol%, based on the total moles of polymerized monomer units in the alpha-olefin-based polymer (AOP); and (iii) a block copolymer (diblock copolymer) having an ethylene block (EB) and an alpha-olefin block (AOB), where the ethylene block of the block copolymer is of the same composition as the EP of component (i) of the specified block composite, and the alpha-olefin block of the block copolymer is of the same composition as the AOP of component (ii) of the specified block composite. In addition, the compositional distribution between the amount of EP and the amount of AOP in the specified block composite will be essentially the same as the compositional distribution between the corresponding blocks in the block copolymer. Non-limiting examples of certain block conjugates of the present disclosure, as well as processes for preparing the same, are disclosed in WO 2017 / 044547, which is incorporated herein by reference in its entirety.

[0025] The term "crystalline block composite" (CBC) refers to a polymer that includes three components: (i) a crystalline ethylene based polymer (CEP) having an ethylene content of greater than 90 mol%, based on the total moles of polymerized monomer units in the crystalline ethylene based polymer (CEP); (ii) a crystalline alpha-olefin based copolymer (CAOP) having an alpha-olefin content of greater than 90 mol%, based on the total moles of polymerized monomer units in the crystalline ethylene based polymer (CEP); and (iii) a block copolymer including a crystalline ethylene block (CEB) and a crystalline alpha-olefin block (CAOB), where the CEB of the block copolymer is of the same composition as the CEP of component (i) of the crystalline block composite, and the CAOB of the block copolymer is of the same composition as the CAOP of component (ii) of the crystalline block composite. In addition, the compositional distribution between the amount of CEP and the amount of CAOP in the crystalline block composite will be essentially the same as the compositional distribution between the corresponding blocks in the block copolymer. Non-limiting examples of the crystalline block composites of the present disclosure, and processes for preparing same, are disclosed in U.S. Pat. No. 8,822,598 (B2) and WO 2016 / 01028961 (A1), which are incorporated herein by reference in their entireties.

[0026] A "propylene-based polymer" is a polymer that contains a majority amount of polymerized propylene, based on the weight of the polymer, and may optionally further contain polymerized units of at least one comonomer. A "propylene-based interpolymer" is an interpolymer that contains a majority amount of propylene in polymerized form, based on the weight of the interpolymer, and further contains polymerized units of at least one comonomer. A "propylene homopolymer" is a polymer that contains repeat units derived from propylene, but does not exclude residual amounts of other components.

[0027] As used herein, the term "propylene / alpha-olefin interpolymer" refers to a polymer that comprises, in polymerized form, a majority weight percent of propylene (based on the weight of the interpolymer) and at least one comonomer that is an alpha-olefin (wherein ethylene is considered an alpha-olefin). The propylene / alpha-olefin interpolymer can be a random or block interpolymer. The term "propylene / alpha-olefin interpolymer" includes the term "propylene / alpha-olefin copolymer."

[0028] As used herein, the term "propylene / alpha-olefin copolymer" refers to a copolymer that includes, in polymerized form, a majority weight percent of propylene (based on the weight of the copolymer) and a comonomer that is an alpha-olefin, where propylene and the alpha-olefin are the only two monomer types. The propylene / alpha-olefin copolymer can be a random or block copolymer.

[0029] The terms "polymeryl", "polymeryl group" and the like refer to a polymer that is missing one hydrogen.

[0030] The terms "polyolefin", "polyolefin group" and the like refer to a polyolefin that is missing one hydrogen.

[0031] Alpha-(halomethyl)acrylates The starting material for step a) of the process of the present disclosure comprises an alpha-(halomethyl)acrylate. In certain embodiments, the alpha-(halomethyl)acrylate has the formula (II):

[0032] [ka] In the formula, X is a halogen; R1 is a C1 to C30 hydrocarbyl group.

[0033] In certain embodiments, X is a halogen and is selected from the group consisting of fluoride, chloride, bromide, and iodide.

[0034] In certain embodiments, R1 is a C1-C30 hydrocarbyl group, which may be linear, branched, or cyclic. In further embodiments, R1 is a C1-C30 alkyl group, which may be linear, branched, or cyclic. For example, R1 can be a linear, branched, or cyclic alkyl group containing 1 to 30 carbon atoms, or 1 to 20 carbon atoms, or 1 to 10 carbon atoms, or 1 to 8 carbon atoms, or 1 to 3 carbon atoms.

[0035] Organoaluminum Compounds The starting material for step a) of the process of the present disclosure comprises an organoaluminum compound of formula R3Al, where each R is independently a C1-C26 hydrocarbyl group or a polyolefinyl group.

[0036] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently a C1-C26 hydrocarbyl group. In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently a C1-C26 hydrocarbyl group, which may be linear, branched, or cyclic. In further embodiments, each R of the organoaluminum compound of formula R3Al is independently a C1-C26 alkyl group, which may be linear, branched, or cyclic. For example, each R of the organoaluminum compound of formula R3Al can independently be a linear, branched, or cyclic alkyl group containing 1 to 26 carbon atoms, or 1 to 10 carbon atoms, or 1 to 8 carbon atoms.

[0037] In some embodiments, each R of the organoaluminum compound of formula R3Al is independently a polyolefinyl group. In further embodiments, each R of the organoaluminum compound of formula R3Al is independently a polyolefinyl group that can be defined by the properties of RH, where RH has a number average molecular weight of greater than 365 g / mol. In further embodiments, each R of the organoaluminum compound of formula R3Al is independently a polyolefinyl group that can be defined by the properties of RH, where RH has a number average molecular weight of greater than 365 g / mol to 10,000,000 g / mol, or greater than 365 g / mol to 5,000,000 g / mol, or greater than 365 g / mol to 1,000,000 g / mol, or greater than 365 g / mol to 750,000 g / mol, or greater than 365 g / mol to 500,000 g / mol, or greater than 365 g / mol to 250,000 g / mol.

[0038] In further embodiments, each R of the organoaluminum compound of the formula RAl is independently a polyolefinyl group that may be defined by the properties of RH, where RH has a density from 0.850 to 0.965 g / cc, or from 0.860 to 0.950 g / cc, or from 0.865 to 0.925 g / cc.

[0039] In further embodiments, each R of the organoaluminum compound of formula RAl is independently a polyolefinyl group that may be defined by the properties of RH, where RH has a melt index (I2) of 0.01 to 2,000 g / 10 min, or 0.01 to 1,500 g / 10 min, or 0.1 to 1,000 g / 10 min, or 0.1 to 500 g / 10 min, or 0.1 to 100 g / 10 min.

[0040] In further embodiments, each R of the organoaluminum compound of the formula RAl is independently a polyolefinyl group that may be defined by the identity of RH, where RH has a number average molecular weight distribution (Mw / Mn or PDI) from 1 to 10, or from 1 to 7, or from 1 to 5, or from 2 to 4.

[0041] In certain embodiments, each R of the organoaluminum compound of the formula R3Al is independently an ethylene homopolymeryl group that includes units derived from ethylene.

[0042] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently an ethylene / alpha-olefin interpolymeryl group comprising units derived from ethylene and at least one C3-C30 alpha-olefin, which can be, for example, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, or 1-octadecene.

[0043] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently an ethylene / alpha-olefin copolymeryl group comprising units derived from ethylene and a C3-C30 alpha-olefin, which can be, for example, propylene, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, or 1-octadecene.

[0044] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently an ethylene / alpha-olefin multiblock interpolymeryl group or an olefin block copolymeryl group, as defined herein.

[0045] In further embodiments, each R of the organoaluminum compound of the formula RAl is independently a polymeryl group of a block complex, a specific block complex, or a crystalline block complex, as defined herein.

[0046] In certain embodiments, each R of the organoaluminum compound of the formula R3Al is independently a propylene homopolymeryl group that includes units derived from propylene.

[0047] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently a propylene / alpha-olefin interpolymeryl group comprising units derived from propylene and at least one comonomer that is ethylene or a C3-C30 alpha-olefin. The C3-C30 alpha-olefin can be, for example, propylene, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, or 1-octadecene.

[0048] In certain embodiments, each R of the organoaluminum compound of formula R3Al is independently a propylene / alpha-olefin copolymeryl group that includes units derived from propylene and a comonomer that is ethylene or a C3-C30 alpha-olefin. The C3-C30 alpha-olefin can be, for example, propylene, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, or 1-octadecene.

[0049] For embodiments in which each R of the organoaluminum compound of formula R3Al is independently a polyolefinyl group, the organoaluminum compound of formula R3Al can be prepared by process (a1), which comprises: i) an olefin monomer component; ii) a catalyst; and iii) combining starting materials including a chain shuttling agent of formula JAl, where each J is independently a C1-C20 hydrocarbyl group; thereby forming a solution or slurry comprising an organoaluminum compound of the formula R3Al.

[0050] The starting material i) olefin monomer component comprises one or more olefin monomers. Suitable olefin monomers include linear or branched alpha-olefins having 2 to 30 carbon atoms, alternatively 2 to 20 carbon atoms, such as ethylene, propylene, 1-butene, 3-methyl-1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, and 1-eicosene; cycloolefins having 3 to 30, alternatively 3 to 20 carbon atoms, such as cyclopentene, cycloheptene, norbornene, 5-methyl-2-norbornene, tetracyclododecene, and 2-methyl-1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalene. Suitable olefin monomers are disclosed, for example, in U.S. Patent No. 7,858,706, column 16, lines 5-36, and U.S. Patent No. 8,053,529, column 12, lines 7-41, which are incorporated herein by reference. In certain embodiments, the starting material i) may comprise ethylene and, optionally, one or more olefin monomers other than ethylene, such as propylene or 1-octene.

[0051] With regard to starting material ii), suitable catalysts include any compound or combination of compounds adapted to prepare a polymer of the desired composition or type. More than one catalyst may be used. For example, a first and a second olefin polymerization catalyst may be used to prepare polymers with different chemical or physical properties. Both heterogeneous and homogeneous catalysts may be used. Examples of heterogeneous catalysts include Ziegler-Natta compositions, particularly Group 4 metal halides supported on Group 2 metal halides or mixed halides, and alkoxides, as well as chromium or vanadium based catalysts. Alternatively, for ease of use and production of narrow molecular weight polymer segments in solution, the catalyst may be a homogeneous catalyst comprising an organometallic compound or metal complex, such as a compound or complex based on a metal selected from Groups 3-15 or the Lanthanide series of the Periodic Table of the Elements. Starting material ii) may further comprise a cocatalyst in addition to the catalyst. The cocatalyst may be a cation forming cocatalyst, a strong Lewis acid, or a combination thereof. Suitable catalysts and cocatalysts are disclosed, for example, in U.S. Pat. No. 7,858,706, column 19, line 45 to column 51, line 29, and in U.S. Pat. No. 8,053,529, column 16, line 37 to column 48, line 17, which are incorporated herein by reference. Suitable procatalysts that may also be added include, but are not limited to, those disclosed in PCT Publication Nos. WO 2005 / 090426, WO 2005 / 090427, WO 2007 / 035485, WO 2009 / 012215, WO 2014 / 105411, WO 2017 / 173080, U.S. Patent Publication Nos. 2006 / 0199930, 2007 / 0167578, 2008 / 0311812, and U.S. Patent Nos. 7,355,089(B2), 8,058,373(B2), and 8,785,554(B2).

[0052] Regarding starting material iii), the chain shuttling agent has the formula JAl, where each J is independently a hydrocarbyl group of 1 to 20 carbon atoms. The hydrocarbyl group of J has 1 to 20 carbon atoms, alternatively 2 to 12 carbon atoms. The hydrocarbyl group of J can be an alkyl group, which can be linear or branched. J can be an alkyl group exemplified by ethyl, propyl, octyl, and combinations thereof. Suitable chain shuttling agents include trialkylaluminum compounds, such as triethylaluminum. Suitable chain shuttling agents are disclosed in U.S. Pat. No. 7,858,706 at column 16, line 37 to column 19, line 44, and in U.S. Pat. No. 8,053,529 at column 12, line 49 to column 14, line 40, which are incorporated herein by reference.

[0053] The starting material for preparing the organoaluminum compound of formula R3Al may optionally further comprise one or more additional starting materials selected from iv) solvents, vi) scavengers, vii) adjuvants, and viii) polymerization aids. Toluene and Isopar™ E are examples of starting material solvents iv). Isopar™ E is an isoparaffinic fluid that typically contains less than 1 ppm benzene and less than 1 ppm sulfur, commercially available from ExxonMobil Chemical Company.

[0054] Process conditions and equipment for preparing organoaluminum compounds of formula R3Al are known in the art and are disclosed, for example, in U.S. Pat. Nos. 7,858,706 and 8,053,529, which are incorporated herein by reference. For example, process (a1) may be characterized as a polymerization that is desirably carried out as a continuous polymerization, preferably a continuous solution polymerization, in which the catalyst components, shuttling agent, monomer, and optionally solvent, adjuvant, removal agent, and polymerization aid are continuously fed to the reaction zone, and the polymer product is continuously removed therefrom. As used in this context, within the scope of the terms "continuous" and "continuously" are those processes in which there is intermittent addition of reactants and removal of products at small regular or irregular intervals, such that over time, the overall process is substantially continuous.

[0055] Polymerization may be advantageously employed as a high pressure, solution, slurry, or gas phase polymerization process. In the case of a solution polymerization process, it is desirable to employ a uniform dispersion of the catalyst components in a liquid diluent in which the polymer is soluble under the polymerization conditions employed. One such process utilizing very fine silica or similar dispersants to produce such a uniform catalyst dispersion when either the metal complex or the cocatalyst is not very soluble is disclosed in U.S. Pat. No. 5,783,512. Solution processes, particularly continuous solution processes, for preparing the novel polymers of the present invention are preferably carried out at temperatures between 80° C. and 250° C., more preferably between 100° C. and 210° C., and most preferably between 110° C. and 210° C. High pressure processes are typically carried out at temperatures between 100° C. and 400° C., and at pressures in excess of 500 bar (50 MPa). Slurry processes may employ an inert hydrocarbon diluent and may employ temperatures from 0° C. to just below the temperature at which the resulting polymer is substantially soluble in the inert polymerization medium. Preferred temperatures in slurry polymerization are from 30° C., preferably from 60° C. up to 115° C., preferably up to 100° C. Pressures typically range from atmospheric (100 kPa) to 500 psi (3.4 MPa).

[0056] Preparation of alpha-substituted acrylates The present process is directed to preparing an alpha-substituted acrylate. In certain embodiments, the alpha-substituted acrylate has the formula (I):

[0057] [ka] In the formula, R is a C1 to C26 hydrocarbyl group or a polyolefinyl group; R1 is a C1 to C30 hydrocarbyl group.

[0058] Each of the R and R groups of the alpha-substituted acrylate of formula (I) is the same as the R group of the organoaluminum compound of formula R3Al and the R group of the alpha-(halomethyl)acrylate of formula (II), respectively, including all embodiments thereof. In fact, the process of the present disclosure relates to a nucleophilic substitution reaction in which X, the halogen, is a leaving group that is replaced by R of the organoaluminum compound of formula R3Al.

[0059] In certain embodiments, step a) of the process of the present disclosure may be carried out appropriately. In further embodiments, the starting material in step a) of the process of the present disclosure further comprises a hydrocarbon solvent. In further embodiments, the starting material in step a) of the process of the present disclosure further comprises a hydrocarbon solvent that is a non-aromatic hydrocarbon solvent.

[0060] In some embodiments, step a) of the process of the present disclosure is carried out at a temperature above the melting temperature of the R group, as defined herein. For example, and without limitation, step a) of the process of the present disclosure may be carried out at a temperature between 15° C. and 100° C.

[0061] In some embodiments, the ratio of alpha-(halomethyl)acrylate to the organoaluminum compound of formula R3Al in step a) is 15:1, or 12:1, or 9:1, or 6:1, or 3:1, or 2:1, or 1:1.

[0062] In preferred embodiments, the processes of the present disclosure exclude any transmetallation steps or reactions.

[0063] In certain embodiments, step a) of the process of the present disclosure is not catalyzed. In further embodiments, step a) of the process of the present disclosure can be catalyzed by one or more organic catalysts. An organic catalyst is a catalyst that excludes any metal element. Thus, in certain embodiments, the starting material in step a) of the process of the present disclosure further comprises an organic catalyst. For example, the starting material in step a) of the process of the present disclosure further comprises a nitrogen-containing heterocycle as disclosed in WO2019 / 182992. The nitrogen-containing heterocycle can be, for example, but not limited to, N-methylimidazole.

[0064] Specific embodiments of the present disclosure include, but are not limited to, the following. Embodiment 1. A process for preparing an alpha-substituted acrylate comprising: a) combining starting materials including an alpha-(halomethyl)acrylate and an organoaluminum compound; thereby forming a product comprising an alpha-substituted acrylate. Embodiment 2. A process for preparing an alpha-substituted acrylate comprising: a) combining starting materials including an alpha-(halomethyl)acrylate and an organoaluminum compound of formula RAl; thereby forming a product comprising an alpha-substituted acrylate; The alpha-substituted acrylate has the formula (I):

[0065] [ka] The alpha-(halomethyl)acrylate has the formula (II):

[0066] [ka] each R is independently a C1 to C26 hydrocarbyl group or a polyolefinyl group; each R1 is independently a C1 to C30 hydrocarbyl group; The process wherein X is a halogen. The process of embodiment 1 or 2, wherein the starting material of embodiment i. step a) further comprises a solvent. Embodiment 4. The process of embodiment 3, wherein the solvent is a non-aromatic hydrocarbon solvent. Embodiment 5. The process of any one of embodiments 1 to 4, wherein the process excludes any transmetallation step or reaction. Embodiment 6. The process of any one of embodiments 1 to 5, wherein the starting material of step a) further comprises an organic catalyst. Embodiment 7. The process of embodiment 6, wherein the organocatalyst is a nitrogen-containing heterocycle. Embodiment 8 The process of embodiment 7, wherein the nitrogen-containing heterocycle is N-methylimidazole. Embodiment 9. The process of any one of embodiments 1 to 8, wherein each R1 is independently a C1-C30, or C1-C10, or C1-C8, or C1-C3 alkyl group that is linear, branched, or cyclic. Embodiment 10. The process of any one of embodiments 1 to 9, wherein each R is independently a C1 to C30 hydrocarbyl group. Embodiment 11. The process of embodiment 10, wherein each R is independently a C1-C30, or C1-C10, or C1-C8 alkyl group that is linear, branched, or cyclic. Embodiment 12. The process of any one of embodiments 1 to 9, wherein each R is independently a polyolefinyl group. Embodiment 13 The process of embodiment 12, wherein the polyolefinyl group is an ethylenic polymeryl group. Embodiment 14. The process of embodiment 13, wherein the polyolefinyl group is an ethylene homopolymeryl group comprising units derived from ethylene. Embodiment 15. The process of embodiment 13, wherein the polyolefinyl group is an ethylene / alpha-olefin interpolymeryl group comprising units derived from ethylene and a C3 to C30 alpha-olefin. Embodiment 16. The process of embodiment 13, wherein the polyolefinyl group is an ethylene / alpha-olefin copolymeryl group comprising units derived from ethylene and a C3 to C30 alpha-olefin. Embodiment 17. The process of embodiment 15 or 16, wherein the C3 to C30 alpha-olefin is selected from the group consisting of propylene, 1-butene, 1-hexene, and 1-octene. Embodiment 18. The process of embodiment 13, wherein the polyolefinyl group is an ethylene / alpha-olefin multiblock interpolymeryl group. Embodiment 19. The process of embodiment 13, wherein the polyolefinyl group is selected from the group consisting of a block complex polymeryl group, a specific block complex polymeryl group, and a crystalline block complex polymeryl group. Embodiment 20 The process of embodiment 12, wherein the polyolefinyl group is a propylene-based polymeryl group. Embodiment 21 The process of embodiment 20, wherein the polyolefinyl group is a propylene homopolymeryl group comprising units derived from propylene. Embodiment 22. The process of embodiment 20, wherein the polyolefinyl group is a propylene / alpha-olefin interpolymeryl group comprising units derived from propylene and either ethylene or a C4 to C30 alpha-olefin. Embodiment 23. The process of embodiment 20, wherein the polyolefinyl group is a propylene / alpha-olefin copolymeryl group comprising units derived from propylene and either ethylene or a C4 to C30 alpha-olefin. Embodiment 24. The process of embodiment 22 or 23, wherein the C4 to C30 alpha-olefins are selected from the group consisting of 1-butene, 1-hexene, and 1-octene. Embodiment 25. The process of any one of embodiments 12 to 24, wherein the polyolefinyl group may be defined by the properties of RH, and RH has a number average molecular weight of greater than 365 g / mol. Embodiment 26. The process according to any one of embodiments 12 to 25, wherein the polyolefin group can be defined by the characteristics of RH, RH having a number average molecular weight of from greater than 365 g / mol to 10,000,000 g / mol, or from greater than 365 g / mol to 5,000,000 g / mol, or from greater than 365 g / mol to 1,000,000 g / mol, or from greater than 365 g / mol to 750,000 g / mol, or from greater than 365 g / mol to 500,000 g / mol, or from greater than 365 g / mol to 250,000 g / mol. Embodiment 27. The process of any one of embodiments 12 to 26, wherein the polyolefin group may be defined by the characteristics of RH, RH having a density of 0.850 to 0.965 g / cc, or 0.860 to 0.950 g / cc, or 0.865 to 0.925 g / cc. Embodiment 28. The process of any one of embodiments 12 to 27, wherein the polyolefinyl group may be defined by the characteristics of RH, RH having a melt index (I2) of 0.01 to 2,000 g / 10 min, or 0.01 to 1,500 g / 10 min, or 0.1 to 1,000 g / 10 min, or 0.1 to 500 g / 10 min, or 0.1 to 100 g / 10 min. Embodiment 29. The process of any one of embodiments 12 to 28, wherein the polyolefin group may be defined by the identity of RH, where RH has a number average molecular weight distribution (Mw / Mn) of 1 to 10, or 1 to 7, or 1 to 5, or 2 to 4. Embodiment 30. The process of any one of embodiments 1 to 29, wherein step a) is carried out at a temperature of 15 to 100° C. Embodiment 31. The process of any one of embodiments 1 to 30, wherein the ratio of alpha-(halomethyl)acrylate to organoaluminum compound in step a) is 15:1, or 12:1, or 9:1, or 6:1, or 3:1, or 2:1, or 1:1. Embodiment 32. The organoaluminum compound is combining starting materials including i) an olefin monomer component, ii) a catalyst, and iii) a chain shuttling agent; 2. The process of embodiment 1, whereby the aluminum oxide is prepared by a process comprising: Embodiment 33. An organoaluminum compound of formula R3Al is combining starting materials including: i) an olefin monomer component; ii) a catalyst; and iii) a chain shuttling agent of formula JAl, where each J is independently a C1-C20 hydrocarbyl group; 32. The process of any one of embodiments 2 to 31, wherein the aluminum compound is prepared by a process comprising:

[0067] Test Method density: Density is measured according to ASTM D-792, Method B.

[0068] Melt Index: Melt index (I2) was measured in accordance with ASTM D-1238, Condition 190° C. / 2.16 kg, which is incorporated herein by reference in its entirety, and is reported in grams dissolved per 10 minutes.

[0069] GPC: Sample polymers were tested for their properties via GPC according to the following:

[0070] A high temperature gel permeation chromatography system (GPC IR) consisting of an infrared concentration detector (IR-5) from PolymerChar Inc (Valencia, Spain) was used for the determination of molecular weight (MW) and molecular weight distribution (MWD). The carrier solvent was 1,2,4-trichlorobenzene (TCB). The autosampler compartment was operated at 160°C and the column compartment at 150°C. The columns used were four Polymer Laboratories Mixed A LS, 20 micron columns. The chromatography solvent (TCB) and sample preparation solvent were from the same solvent source with 250 ppm butylated hydroxytoluene (BHT) and sparged with nitrogen. Samples were prepared at a concentration of 2 mg / mL in TCB. The polymer samples were gently shaken at 160°C for 2 hours. The injection volume was 200 μL and the flow rate was 1.0 ml / min.

[0071] Calibration of the GPC column set was performed with 21 narrow molecular weight distribution polystyrene standards, ranging from 580 to 8,400,000 g / mol, arranged in six "cocktail" mixtures with at least one order of magnitude between individual molecular weights.

[0072] Prior to running the examples, the GPC column set was calibrated by running 21 narrow molecular weight distribution polystyrene standards. The molecular weights (Mw) of the standards ranged from 580-8,400,000 grams per mole (g / mol) and the standards were contained in six "cocktail" mixtures. Each standard mixture had at least one order of magnitude between the individual molecular weights. The standard mixtures were purchased from Polymer Laboratories (Shropshire, UK). The polystyrene standards were prepared at 0.025 g in 50 mL of solvent for molecular weights equal to or greater than 1,000,000 g / mol and 0.05 g in 50 mL of solvent for molecular weights less than 1,000,000 g / mol. The polystyrene standards were dissolved at 80° C. for 30 minutes with gentle agitation. The narrow standard mixtures were run first and in order of decreasing highest molecular weight (Mw) components to minimize degradation. The polystyrene standard peak molecular weights were converted to polyethylene Mw using the Mark-Houwink constants. Once the constants were obtained, the two values ​​were used to construct two linear standard calibrations for polyethylene molecular weight and polyethylene intrinsic viscosity as a function of elution column.

[0073] Polystyrene standard peak molecular weights were converted to polyethylene molecular weights using the following formula (as described in Williams and Ward, J. Polym. Sci., Polym. Let., 6, 621 (1968)): M ポリエチレン =A(M ポリスチレン ) B (1) where B has a value of 1.0 and the experimentally determined value of A is approximately 0.41.

[0074] A third order polynomial was used to fit each of the polyethylene equivalent calibration points obtained from equation (1) to their observed elution deposits of the polystyrene standards.

[0075] The number average, weight average, and z average molecular weights were calculated according to the following formulas:

[0076] [ka] In the formula, Wf i is the weight fraction of the i-th component, and M i is the molecular weight of the i-th component.

[0077] MWD was expressed as the ratio of weight average molecular weight (Mw) to number average molecular weight (Mn).

[0078] The exact A value was determined by adjusting the A value in equation (1) until the Mw and corresponding retention deposition polynomial calculated using equation (3) matched the known Mw value of a standard linear polyethylene homopolymer reference, 120,000 g / mol.

[0079] The GPC system consisted of a Waters (Milford, Mass.) 150° C. high temperature chromatograph (other suitable high temperature GPC equipment includes Polymer Laboratories (Shropshire, UK) Model 210 and Model 220) equipped with an on-board refractive index detector (RI). Additional detectors may include a Polymer ChAR (Valencia, Spain) IR4 infrared detector, a Precision Detectors (Amherst, Mass.) two-angle laser light scattering detector model 2040, and a Viscotek (Houston, Tex.) 150R 4-capillary solution viscometer. GPC with the last two independent detectors and at least one first detector is sometimes referred to as "3D-GPC", although the term "GPC" alone generally refers to conventional GPC. Depending on the sample, either a 15 degree angle or a 90 degree angle of the light scattering detector was used for calculation purposes.

[0080] Data collection was performed using Viscotek TriSEC software, version 3, and a Viscotek Data Manager DM400 with four channels. The system was also equipped with an online solvent degassing device from Polymer Laboratories (Shropshire, UK). A suitable high temperature GPC (MixA LS, Polymer Lab) column could be used, such as four 30 cm long Shodex HT803 13 micron columns or four 30 cm long Polymer Lab columns with 20 micron mixed pore size packings. The sample carousel compartment was operated at 140°C and the column compartment was operated at 150°C. Samples were prepared at a concentration of 0.1 grams of polymer in 50 milliliters of solvent. The chromatographic solvent and sample preparation solvent contain 200 ppm butylated hydroxytoluene (BHT). Both solvents were sparged with nitrogen. The polyethylene samples were gently stirred at 160°C for four hours (4 h). The injection volume was 200 microliters (μL). The flow rate through the GPC was set at 1 mL / min.

[0081] NMR( 13 C and 1 H): NMR analyses were carried out at room temperature using standard NMR solvents such as chloroform or benzene and data were acquired on a Varian 500 MHz spectrometer.

[0082] GCMS: Tandem gas chromatography / low resolution mass spectrometry with electron impact ionization (EI) is performed on an Agilent Technologies 6890N series gas chromatograph equipped with an Agilent Technologies 5975 inert XL mass selective detector and an Agilent Technologies Capillary column (HP1MS, 15 m×0.25 mm, 0.25 micron) at 70 eV for the following:

[0083] Programmed Method: Oven equilibration time of 0.5 min at 50°C Then 25°C / min to 200°C and hold for 5 min Run time 11 minutes EXAMPLES

[0084] The following examples are intended to illustrate some embodiments of the invention and should not be construed as limiting the scope of the invention as set forth in the claims.

[0085] Unless otherwise stated, all materials and reagents are commercially available, such as from Sigma Aldrich.

[0086] Example 1

[0087] [ka] The reaction of Example 1 was carried out under an inert nitrogen atmosphere glove box according to the exemplary and non-limiting reaction scheme above. To a solution of ethyl bromomethyl acrylate (193 mg) in dry methylcyclohexane (5 mL) in a 20 mL vial, a solution of Oct3Al (122.5 mg, 0.33 equiv.) was slowly added at room temperature. The reaction mixture turned slightly yellow and the color disappeared after overnight at room temperature. 1,3,5-tribromobenzene was added (76 mg, 0.244 mmol) as an internal standard.

[0088] After 12 hours at room temperature, the NMR conversion was calculated to be about 35%, as seen in FIG. 1A.

[0089] The reaction mixture was further heated at 85° C. for 6 h. NMR indicated approximately 60% conversion with the formation of some by-products, as seen in FIG. 1B. Integration versus internal standard gave a 61% NMR yield. Further heating did not improve the conversion, but more by-products were formed.

[0090] Example 2

[0091] [ka] The reaction of Example 2 was carried out under an inert nitrogen atmosphere glove box according to the non-limiting and exemplary reaction scheme above. A solution of Oct3Al (136.5 mg, 0.33 equiv.) was slowly added at room temperature to a solution of methylchloromethylacrylate (134.6 mg) in dry methylcyclohexane (5 mL) in a 20 mL vial. The reaction mixture turned slightly yellow and the color disappeared after overnight at room temperature. 1,3,5-tribromobenzene (71.7 mg, 0.227 mmol) was added as an internal standard.

[0092] After 12 hours at room temperature, the NMR conversion was calculated to be about 39%, as seen in FIG. 2A.

[0093] The reaction mixture was further heated at 85 °C for 6 h. NMR indicated about 56% conversion with the formation of some by-products, as seen in Figure 2B. Integration versus internal standard gave 46-50% NMR yield. Further heating did not improve the conversion, but more by-products were formed.

Claims

1. 1. A process for preparing an alpha-substituted acrylate comprising: a) alpha-(halomethyl)acrylate and a compound of formula R ３ combining starting materials including an organoaluminum compound of Al; thereby forming a product comprising said alpha-substituted acrylate; The alpha-substituted acrylate has the formula (I): 【Chemistry 1】 The alpha-(halomethyl)acrylate has the formula (II): 【Chemistry 2】 each R is independently a C1 to C26 hydrocarbyl group or a polyolefinyl group; each R1 is independently a C1 to C30 hydrocarbyl group; X is a halogen; The process excludes a transmetallation step or reaction.

2. 10. The process of claim 1, wherein the starting material of step a) further comprises a solvent.

3. 3. The process of claim 2, wherein the solvent is a non-aromatic hydrocarbon solvent.

4. The process according to any one of claims 1 to 3, wherein the starting material of step a) further comprises an organic catalyst.

5. The process of any one of claims 1 to 4, wherein each R is independently a C1 to C26 hydrocarbyl group.

6. 5. The process of any one of claims 1 to 4, wherein each R is independently a polyolefinyl group that may be defined by the properties of R-H, where R-H has a number average molecular weight greater than 365 g / mol.

7. 7. The process of claim 6, wherein the polyolefinyl group is an ethylenic polymeryl group.

8. 8. The process of claim 7, wherein the polyolefinyl group is an ethylene homopolymeryl group comprising units derived from ethylene.

9. The process of claim 7, wherein the polyolefinyl group is an ethylene / alpha-olefin interpolymeryl group comprising units derived from ethylene and a C3 to C30 alpha-olefin.

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