163 results about "Halohydrin" patented technology

A process for producing epoxides, the process including: (a) feeding at least one aqueous alkali and at least one halohydrin to a reactive distillation column, wherein the reactive distillation column includes a feed zone, a top zone disposed above the feed zone, and a bottom zone disposed below the feed zone; (b) concurrently in the reactive distillation column: (i) reacting at least a portion of the halohydrin with the alkali to form an epoxide; and (ii) stripping water and the epoxide from a basic aqueous residue; (c) recovering the water and the epoxide from the reactive distillation column as an overheads fraction; (d) condensing and phase separating the overheads fraction to form an organic overheads fraction including the epoxide and an aqueous overheads fraction including water; and (e) maintaining a liquid holdup per plate in the feed zone at a residence time of 10 seconds or less.

The present invention provides a process for eliminating contaminants from epihalohydrin-derived epoxy resins. Another embodiment of the present invention is an epoxy product formed using said process. Yet another embodiment of the present invention is an epoxy derived in part from epihalohydrin wherein said epoxy is has a hydrolyzable halogen content of less than 10 ppm and an epoxide equivalent weight within 2 percent of the theoretical epoxide equivalent weight.

A process for manufacturing an α-dihydroxy derivative from an aryl allyl ether wherein such α-dihydroxy derivative can be used to prepare an α-halohydrin intermediate and an epoxy resin prepared therefrom including epoxidizing an α-halohydrin intermediate produced from a halide substitution of an α-dihydroxy derivative which has been obtained by a dihydroxylation reaction of an aryl allyl ether in the presence of an oxidant or in the presence of an oxidant and a catalyst.

A composition comprising one or more high molecular weight resins and one or more low molecular weight resins in a ratio of about 1:99 to about 99:1 based on polymer actives, wherein said high molecular weight resins are selected from the group consisting of glyoxylated polyacrylamide, crosslinked polyaminoamide and polyaminoamide-epihalohydrin resins having a molecular weight of about 100,000 to about 5,000,000 Dalton and the low molecular weight resins are selected from the group consisting of glyoxylated polyacrylamide, crosslinked polyaminoamide and polyaminoamide-epihalohydrin resins having a molecular weight of less than about 100,000 Dalton and wherein the mole ratio of epihalohydrin to secondary nitrogen atoms in the high and low molecular weight polyaminoamide-epihalohydrin resins is less than about 0.5. and use of the composition for creping paper webs.

A process for preparing regioselectively an optically active 1-halogeno-2-hydroxypropyl compound of the following formula;

• • wherein X is halogen atom and Nu is a heteroatom having a substituent,

and an optically active glycidyl compound of the formula;

which comprises reacting an optically active epihalohydrin of the formula;

with a neucleophilic agent,

in the presence of a metal complex of the formula;

wherein n is an integer of 0, 1 or 2, Y¹, Y² and Y³ are hydrogen atom, etc., and Y² and Y³ may form a ring such as benzene, A is a counterion and M is a metal ion, and further subjecting the compound (4) to reaction with a base to prepare the optically active glycidyl compound (5).

The invention relates to the field of organic synthesis and provides a phosphorus-containing flame retardant and a preparation method thereof. The phosphorus-containing flame retardant has a chemical formula shown as a formula (i). The preparation method comprises the following steps: (1) adding DOPO and dicarboxylic acid into toluene, stirring and heating to 110+/-2 DEG C, reacting for 2-6 hours, stopping heating, performing suction filtration on the reacted solution, obtaining white solids, drying, and preparing a DOPO dicarboxylic acid derivative; (2) dissolving the DOPO dicarboxylic acid derivative in a 2+/-0.2 mol/L of potassium hydroxide solution at the temperature of 0-40 DEG C, stirring for 1.5-2.5 hours, and generating sylvite of the DOPO dicarboxylic acid derivative; (3) adding a phase transfer catalyst and halohydrin into the solution prepared in the step (2), reacting for 4-8 hours, layering the solution in a separating funnel, taking the lower layer, and obtaining the phosphorus-containing flame retardant. (img file='2014100188078100004dest-path-image001.TIF' wi='366' he='207' /) (i).

The invention is directed towards methods and compositions for improving the sizing of paper using PAE. Proper sizing of paper requires that a sizing agent adequately disperse so as to evenly distribute on the paper. Proper sizing also requires that the agent not cause runnability or chemical problems with other materials or equipment used in the papermaking process. PAE displays unexpected attributes that allow it to disperse sizing agents. Best of all it is not subject to the same overdose effect of typical emulsifiers such as cationic starch. As a result PAE is an excellent option for use in sizing paper.

The invention discloses a polymerizable type thioxanthone visible light initiator containing acrylate or methacrylate and a preparation method of the polymerizable type thioxanthone visible light initiator. Thioxanthone containing an aromatic amino group can be directly reacted with various types of halogenated alcohol to generate thioxanthone containing an aliphatic hydroxyl group; the thioxanthone containing the aromatic amino group can also be reacted with 4-benzoyloxy benzyl chloride, and then is subjected to alcoholysis to generate thioxanthone containing a phenolic hydroxyl group; the thioxanthone containing the phenolic hydroxyl group can be reacted with the various types of halogenated alcohol to generate thioxanthone containing the aliphatic hydroxyl group; then the thioxanthone containing the phenolic hydroxyl group or the thioxanthone containing the aliphatic hydroxyl group is reacted with acryloyl chloride or methacryloyl chloride to form the polymerizable type thioxanthone visible light initiator containing an acrylate structure or a methacrylate structure. The compound disclosed by the invention has very good compatibility with a light curing system; in an application process, any additive does not need to be added, and any auxiliary agent does not need to be added; the polymerizable type thioxanthone visible light initiator is high in initiation efficiency, green and environment-friendly and low in energy consumption, meets the requirements of green chemistry, and has a wide application prospect in the field of visible light curing.

A process for producing epoxide, the process including contacting an organic phase including at least one halohydrin(s) with at least one aqueous phase including a base in a plug-flow mixer/reactor system to disperse the organic phase in the aqueous phase via a mixing device imparting a power-to-mass ratio of at least 0.2 W/kg to convert at least a portion of the at least one halohydrin to an epoxide.

The present invention relates to (meth)acrylated compounds (A) prepared from (a) at least one cyclic ether polyol, (b) at least one linking compound (b1) and/or (b2), wherein the linking compound (b1) is selected from cyclic compounds (b11) containing at least one (I) group in the cycle where X=O or NH, from hydroxy acids (b12) and/or from alkylene oxides (b13) containing from 2 to 4 carbon atoms and the linking compound (b2) is selected from epihalohydrins or polyisocyanates, (c) a (meth)acrylating compound; and to their use in radiation curable compositions for the coatings, inks, overprint varnishes, adhesives and composites.

The invention provides a preparation method for tert-carbonic acid glycidyl ester. The tert-carbonic acid glycidyl ester is synthesized through two steps, i.e., a first step of subjecting tert-carbonic acid and a halogenated epoxy compound to a reaction under the action of a catalyst to produce tert-carbonic acid halohydrin ester and a second step of removing halogen hydride from the tert-carbonic acid halohydrin ester to form the tert-carbonic acid glycidyl ester, wherein in the first step of synthesis of the tert-carbonic acid halohydrin ester, the tert-carbonic acid reacts with the halogenated epoxy compound only in the presence of water and the catalyst and the water comprises water added in the reaction in advance. With the preparation method provided by the invention, product output per unit volume can be substantially increased, and the method is especially applicable to large-scale industrial production of tert-carbonic acid glycidyl ester with low cost, high purity and a light and stable color.

An epoxy resin adduct including the reaction product of (A) at least one polyfunctional aliphatic or cycloaliphatic epoxy resin; and (B) at least one reactive compound; wherein the polyfunctional aliphatic or cycloaliphatic epoxy resin is isolated from the epoxy resin formed by the epoxidation of (i) an aliphatic or cycloaliphatic hydroxyl-containing material using (ii) an epi-halohydrin, (iii) a basic-acting substance, (iv) a non-Lewis acid catalyst, and (v) optionally one or more solvents; and wherein the re-active compound (B) comprises one or more compounds having two or more reactive hydrogen atoms per molecule and the reactive hydrogen atoms are reactive with epoxide groups. A curable epoxy resin composition includes the adduct described above. A cured epoxy resin is prepared by a process of curing the curable epoxy resin composition containing the adduct described above.

The present invention is a catalyst component for ethylene polymerization, which is formed by dissolving magnesium halide in organic epoxy compounds and organic phosphorus compounds to form a uniform solution, adding halogenated alcohols and alcohols, and in the presence of organosilicon compounds without active hydrogen in the precipitation aid Under the role of titanium compounds obtained. Due to the addition of halohydrin compounds, the catalyst exhibits higher polymerization activity, better hydrogen adjustment sensitivity and better bulk density when used in ethylene polymerization. And adopt the organosilicon compound without active hydrogen as precipitation aid, help to improve the activity of catalyst and the improvement of the particle form of catalyst, the catalyst particle form of preparation is better; Do not need to use a large amount of titanium tetrachloride to promote precipitation Precipitation and repeated use of titanium tetrachloride to deal with the precipitate resulted in a significant reduction in the amount of titanium tetrachloride added.

The invention discloses a method for synthetizing a hydrogenated bisphenol A epoxy resin under the catalysis of ammonium salt. According to the method, epihalohydrin such as hydrogenated bisphenol A, epichlorohydrin and the like are taken as raw materials, simultaneously, an ammonium salt catalyst and alkali are added, a ring-opening etherification reaction is performed at the temperature of 30 DEG C-100DEG C, and halogen alcohol ether is obtained; then, the alkali is continuously added in the same reaction system, and a ring-closing epoxidation reaction is performed at the temperature of 20 DEG C-80 DEG C; and the hydrogenated bisphenol A epoxy resin is obtained through posttreatment processes such as filtering, washing, separation, reduced pressure distillation and the like. A product is measured to be superior to number one with a GB-T12007.1-1989 epoxy resin color measuring method-Gardner colorimetric method.

The invention relates to an organosilicon emulsion containing elastic body polyorganosiloxane with quaternary ammonium functionality and polydiorganosiloxane with a non-reactivity organic group. The organosilicon emulsion is obtained through the following method: in the presence of the polydiorganosiloxane with the non-reactivity organic group not reacting with other components (such as polyorganosiloxane with an amino group, an organic quaternary ammonium compound and a crosslinking agent) and a surfactant, the polyorganosiloxane with the amino group and the organic quaternary ammonium compound with an epoxy group or a halohydrin group react simultaneously, the crosslinking agent is used to crossly link the polyorganosiloxane with the amino group, and the components are dispersed in a polarity water phase. The organosilicon emulsion can be applied to various fields of textile fabrics, personnel nursing articles, and the like.

Accordingly, the invention relates to a process for the preparation of a glycidyl ester of a branched monocarboxylic acid by reacting an aliphatic monocarboxylic acid of the formula R¹R²R³COOH, wherein R¹, R², and R³ each independently represent an alkyl radical of normal or branched structure containing from 1 to 20 carbon atoms and an epoxyalkyl halide containing from 3 to 13 carbon atoms in the presence of a catalyst, wherein

• • a greater than stoichiometric amount of epoxyalkyl halide is reacted with the acid
  • (e.g., preferably in the molar ratio of epoxyalkyl halide to acid that is in the range of from 1.02:1 to 1.50:1) to form an intermediate reaction product comprising a halohydrin,
  • the epoxyalkyl halide is added to the acid with appropriate cooling of the reactants and/or the reaction mixture to keep the temperature of the reaction mixture below 80° C., whereupon the epoxyalkyl halide and the acid are reacted at a temperature below 80° C. (preferably in the range of from 55 to 75° C.) for a time sufficient to reduce the amount of acid to no more than 2 wt % but no less than 0.1 wt % calculated on the initial amount of acid,
  • optionally removing any excess epoxyalkyl halide from the reaction product prior to the ring closure reaction,
  • subjecting the reaction product to a ring closure reaction (DHC) and optionally to one or more after treatments (ADHC) for removal of any remaining halo functionality.

A process for easily producing various optically active chroman derivatives that are useful as pharmaceutical intermediates from inexpensive starting materials is provided.

Cyclic hemiacetal (1) obtained from dihydrocoumarin through one step is asymmetrically reduced to produce an optically active halohydrin derivative (3), and the optically active halohydrin derivative (3) is cyclized to produce an optically active chroman derivative (13):

A method for fluoromethylation of a halogenated alcohol. The method includes refluxing a halogenated alcohol with a dihalomethane under basic conditions in a first solvent to form a halomethyl ether and fluorinating the halomethyl ether in the presence of a fluorinating agent.

The invention relates to a method for preparing a gefitinib intermediate, in particular to a method for preparing 4-chlorine-6-(3-chlorine propoxy)-7-methoxy quinazoline. A formula II compound 6-(3-hydroxy propoxy)-7-methoxy quinazoline-4 (3H)-ketone and thionyl chloride are reacted to obtain the gefitinib intermediate. The formula II compound uses 5-hydroxy-4-methoxy group-2-nitrobenzene methyl formate as a raw material to be condensed with halohydrin shown in a formula VI, nitro is reduced, and formamidine acetate cyclization and thionyl chloride chlorination are reacted to obtain the gefitinib intermediate. The synthesis scheme provided by the invention reduces the generation of by-products by introduction of hydroxyl, the production cost is reduced, meanwhile, the environment pollution is reduced, the quality of products is increased, and the purity of the prepared 4-chlorine-6-(3-chlorine propoxy)-7-methoxy quinazoline is over 98 percent. Compared with the prior art, the method is greatly increased and improved, wherein, X is halogen.

The invention provides a catalyst system for ethylene polymerization or copolymerization. The catalyst system comprises a solid catalyst component (A) and a solid catalyst component (B). A magnesium halide is dissolved in an organic alcohol to form a uniform solution and the solution reacts with a halide of transition metal titanium or its derivative and a reactive hydrogen-free organosilicon compound to produce the solid catalyst component (A). An aluminum alkyl compound and a halohydrin are mixed into the solid catalyst component (B). The catalyst system is used for ethylene polymerization or copolymerization and has characteristics of high activity, high bulk density and good catalyst hydrogen regulation sensitivity.

The purpose of the present invention is to provide: a photosensitive epoxy resin composition and/or a resist laminate of said resin composition that makes it possible to use photolithography to form an image having a vertical sidewall shape and fine resolution, low stress, and heat/humidity resistance; and a cured product of said resin composition and said resist laminate. The present invention is a photosensitive resin composition comprising: (A) an epoxy resin; (B) a polyphenol compound having a specific structure; (C) a photocationic polymerization initiator; and (D) an epoxy group-containing silane compound. The epoxy resin (A) comprises: an epoxy resin (a) obtained by reacting a phenol derivative that is represented by formula (1) with an epihalohydrin; and an epoxy resin (b) that is represented by formula (2).