106 results about "2-imidazolidinone" patented technology

A polishing composition which achieves surfaces with high planarity and the reduction of corrosions in the wiring metal surface at the same time is provided.

Such compositions include

• • (A) an oxidizing agent;
  • (B) at least one acid selected from an amino acid, a carboxylic acid of no more than 8 carbon atoms, and an inorganic acid;
  • (C) a sulfonic acid having a concentration of 0.01% by mass or more and having an alkyl group of 8 or more carbon atoms;
  • (D) a fatty acid having a concentration of 0.001% by mass or more and having an alkyl group of 8 or more carbon atoms; and
  • (E) at least one compound selected from a pyridine carbonyl compound, a nonionic water-soluble polymer, 2-pyrrolidone, N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, gramine, adenine, N,N′-diisopropylethylenediamine, N,N′-bis(2-hydroxyethyl)ethylenediamine, N,N′-dibenzylethylenediamine, and N,N′-diphenylethylenediamine.

A primary cell having an anode comprising lithium and a cathode comprising iron disulfide (FeS₂) and carbon particles. The electrolyte comprises a lithium salt dissolved in a solvent mixture which contains 1,3-dioxolane and preferably 1,3-dimethyl-2-imidazolidinone. A cathode slurry is prepared comprising iron disulfide powder, carbon, binder, and a liquid solvent. The mixture is coated onto a conductive substrate and solvent evaporated leaving a dry cathode coating on the substrate. The anode and cathode can be spirally wound with separator therebetween and inserted into the cell casing with electrolyte then added.

The present invention addresses the problem of providing a water-based coating agent composition (in particular, a water-based lubricating film paint composition that includes a solid lubricant) that suppresses the interaction of a curable resin and a surfactant, that suppresses thickening/disproportionation throughout a water-based coating agent, that has superior total fluidity, coating properties, and storage stability, and that can form a favorable coating film, and the problem of providing a member that is provided with said coating film, and a method for forming said coating film. Said problems can be solved by a water-based coating agent composition that includes (A) a curable resin in the form of a water-based emulsion, (B) a surfactant, (C) solid particles, (D) one or more nitrogen-containing heterocyclic compound, and (E) water. In particular, the (C) component preferably includes a solid lubricant, and for reasons of environmental regulations, it is particularly preferable that the (D) component be 1,3-dimethyl-2-imidazolidinone.

The invention relates to a liquid crystal orientation agent, a liquid crystal orientation film, a manufacturing method of the liquid crystal orientation film, and a liquid crystal display element. The liquid crystal orientation agent has good printing performance with respect to a substrate and good continuous printing performance and prevents swelling of printing plates. The liquid crystal orientation agent contains at last one polymer (A) selected from the group formed by polyamide acid, polyimide, polyamide acid ester and polysiloxane, a first solvent containing more than one of N-ethyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolone, 3-methoxy-N, N-dimethylpropionamide and so on, and a second solvent containing more than one of propylene glycol diacetate, diethylene glycol diethyl ether, diisoamyl ether diacetone alcohol and so on.

The invention relates to a preparation method for full saccharose polyether polyol, belonging to the technical field of synthesis of polyether polyol. According to the preparation method, only saccharose is taken as an initiator, a catalyst KOH is solvated by 1, 3-dimethyl-2-imidazolone and then is reacted with epoxypropane. The preparation method for full saccharose polyether polyol improves the alcohol and potassium preparation process. The prepared polyether polyol has high degree of functionality and strength, so that the compound material prepared by the polyether polyol can resist low temperature minus 86DEG C when the normal molding density is about 40Kg/m<3>, the overall injection quantity is about 50% lower than that of a normal hard bubble compound polyether system, and the polyether polyol has low cost and high cost performance, and the use field of hard polyurethane foaming plastics is enlarged.

The invention discloses a process for synthesizing 3,4-difluorobenzonitrile. According to the process, 3,4-difluorobenzonitrile with the purity of over 99% is obtained through taking 3,4-dichlorobenzonitrile as a raw material, taking potassium fluoride as a fluorination reagent, taking 1,3-dimethyl-2-imidazolidinone as a reaction solvent, taking bis-(N-bis(dimethylamino)methylene)-iminium chloride as a catalyst, enabling reactants to react for 2-3 hours at the temperature of 130-150 DEG C and react for 5-6 hours at the temperature of 180-200 DEG C, then ending reaction, filtering a reaction solution and then rectifying under reduced pressure, and the yield can reach 85%. Rectification mother liquor (containing the catalyst) is mechanically applied to next-batch reaction directly. According to the process disclosed by the invention, the raw material is easy to obtain, the reaction conditions are mild, the reaction time is short, the operation is simple, the yield is high, the reaction solvent (containing the catalyst) can be repeatedly applied mechanically, the cost is low, and the emission of waste gases, waste water and waste residues is little, so that the process is applicable to industrial production.

Disclosed is a process for preparing mezlocillin sodium belonging to compound preparation technical field. By acylation reaction of aminobenzyl triaqua acid with 1-chloroformyl-3-mesyl-2-imidazolidinone, acidizing after an ethyl acetate solvent being added, esterified layer removing, salifying reaction after a sodium salt forming agent being added, and seedout, the mezlocillin sodium is obtained. In the invention, the mixed solvent is adopted and the speed of adding the sodium salt forming agent is adjusted. There is recrystallization buffer, so the crystal grain is big and the purity is high.

Disclosed is an ink composition including: (1) a pigment; (2) a polymerization initiator having a content of 2% by mass or more with respect to a total amount of the composition and having a solubility with respect to pure water at 25° C. of 5 to 8 g/l; (3) a compound A that is at least one selected from the group consisting of dimethylacrylamide, diethylacrylamide, N-isopropylacrylamide, dimethylacetamide, N-ethylpyrrolidone, 1-cyclohexyl-2-pyrrolidone, 1-(2-hydroxyethyl)-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinone, tetramethylurea and gamma-valerolactone; (4) a polymerizable compound having two or more ethylenically unsaturated double bonds; and (5) water having a content of 50% by mass or more with respect to the total amount of the composition.

This invention relates to synthetic method of 1, 3 - dimethyl - 2-imidazolidinone. The invention solves the problem in exsiting method that the reaction need 85% concentration methanoic acid as reaction medium, and the generated methanoic acid has no means of reusing. The invention takes paraformaldehyde and 2-imidazolidinone as raw material, 30% to 45%methanoic acid as reaction medium. Firstly proceed paraformaldehyde depolymerization, then add 85%or 94% methanoic acid, warm-up till circumfluence reaction for 12 hours, then gain 1, 3 - dimethyl - 2-imidazolidinone. The invention could cyclic utilize sparse methanoic acid generated from 1, 3 - dimethyl - 2-imidazolidinone synthetic reaction, thereby advance capacity utilization rate, depress manufacturing cost.

Disclosed is a process for producing a polyimide film, which comprises applying a polyamic acid solution composition to a base material to form a coating film, and subsequently heating the coating film, wherein the polyamic acid solution composition comprises a mixed solvent of two or more solvents selected from N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone and 1,3-dimethyl-2-imidazolidinone (wherein each of the solvents is contained in an amount of 7 to 93 mass% relative to 100 mass% of the total amount of the solvents) and a polyamic acid mainly composed of s-BPDA and PPD. The process enables to produce a polyimide film having a film thickness of more than 40 [mu]m without the need of expanding the film.

The invention relates to a preparation process of Mezlocillin, which reacts Ampicillin trihydrate with 1-chlorocarbonyl-3-methylsulfonyl-2-imidazolidinone in water phase under alkaline condition and then proceeds acidified crystallization, filtration, washing and drying in acetone/water, or alcohol/water, or isopropanol/water system to obtain Mezlocillin. The Mezlocillin prepared by the inventive method can reach 95%-97% of molar yield, 0.06%-0.4% of organic residual quantity, more than 98.5% of dry basis content, less than 0.4% of single impurity, less than 1.5% of total related substances and good quality, is particularly suitable for direct lyophilization in water-phase salt formation to obtain high-quality Mezlocillin sodium for injection of medicinal product, and has prominent economical and social benefits.

Disclosed is an emulsifiable concentrate composition characterized by containing not less than 0.5% by weight but not more than 25% by weight of a hydrophobic agrochemically active compound, not less than 5% by weight but not more than 15% by weight of a surfactant, not less than 2% by weight but not more than 60% by weight of an aromatic hydrocarbon solvent, not less than 2% by weight but not more than 60% by weight of γ-butyrolactone, and not less than 12% by weight but not more than 90% by weight of 1,3-dimethyl-2-imidazolidinone. The emulsifiable concentrate composition is also characterized in that the weight ratio of 1,3-dimethyl-2-imidazolidinone to γ-butyrolactone, namely (1,3-dimethyl-2-imidazolidinone):(γ-butyrolactone) is within the range from 1:0.03 to 1:2.

There is provided a liquid agrochemical composition having a stable water-diluted state, which comprises 0.5 to 30% by weight of one or more hydrophobic agrochemical active compounds, 1 to 20% by weight of one or more nonionic surfactants selected from the group consisting of a polyoxyethylene polyoxypropylene block copolymer and the like, 0 to 10% by weight of one or more anionic surfactants, 6 to 60% by weight of an ether compound represented by R<1>-O-A<1>-O-A<2>-(O-A<3>)n-O-R<2>, wherein R<1 >and R<2 >represent a C1-3 alkyl group, A<1>, A<2 >and A<3 >represent an ethylene group or a propylene group, and n represents 0, 1 or 2, and 20 to 75% by weight of 1,3-dimethyl-2-imidazolidinone.

A nonaqueous ink-jet ink comprising at least solvents (A) and (B) cited below, a pigment, and a polymer compound, wherein the content of solvent (A) is 3-15% by weight based on the total weight of the ink-jet ink, and the content of solvent (B) is 50-90% by weight: Solvent (A): 1,3-dimethyl-2-imidazolidinone; Solvent (B): a solvent comprising at least one compound selected from the group consisting of the compounds represented by following Formulas (1) and (2): Formula (1) R¹—(OX¹)₂—O—R², and

The invention discloses a preparation method of methyl-2,3-O-isopropylidene-5-deoxy-D-ribofuranoside. The method comprises: taking D-ribose as an initial material to obtain methyl-2,3-O-isopropylidene-D-ribofuranoside under the protection of methanol/acetone; reacting methyl-2,3-O-isopropylidene-D-ribofuranoside with paratoluensulfonyl chloride to obtain methyl-2,3-O-isopropylidene-5-O-paratoluenesulfonyl-D-ribofuranoside in alkaline condition, wherein the reaction is subjected to proper treatment and needs no purification; taking hexamethylphosphoric triamide or N,N-dimethyl-2-imidazolidinone as a reducing solvent; and using hydroboron for reduction to obtain methyl-2,3-O-isopropylidene-5-deoxy-D-ribofuranoside. The reducing reaction agent can be recycled; the reaction intermediates are subjected to proper treatment and need no purification; and the preparation method is simple to operate, wild in condition, and low in production cost.

The invention discloses a synthesis method of 1,3-dimethyl-2-imidazolone. The method comprises steps as follows: (1) montmorillonite, palladium on carbon, 2-imidazolidone and a formaldehyde water solution are sequentially added to a heatable and inflatable autoclave, and hydrogen is introduced into the autoclave for a reaction at the temperature of 110-160 DEG C for 1-5 h; (2) a material obtainedin the step (1) is filtered to recover montmorillonite and palladium on carbon, remaining formaldehyde and by-product water in filtrate are removed through distillation after the filtrate is collected, and a crude product is obtained; (3) the crude product is purified by rectification, and 1,3-dimethyl-2-imidazolone is obtained. The used catalyst is montmorillonite which is low in cost, can be directly used without further treatment or modification and is easy to recycle.

The invention discloses a method for preparing sertindole, which belongs to the technical field of organic synthesis. The method comprises the following steps of: using alkyl imidazole type ionic liquid as a solvent; and under the catalysis of a solid base, reacting 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridine-4-yl)-1H-indole (IA) or a salt thereof, or 5-chloro-1-(4-fluorophenyl)-3-(4-piperidinyl)-1H-indole (IB) or a salt thereof with 1-(2-chloroethyl)-2-imidazole azululanone (II) to generate 1-[2-[4-[5-chloro-1-(4-fluorophenyl)-1-H-indole-3-yl]-5,6-dihydro-piperidine-1(2H)-yl]ethyl]-2-imidazolidinone (IIIA) or 1-[2-[4-[5-chloro-1-(4-fluorophenyl)-1-H-indole-3-yl]-1-piperidinyl]ethyl]-2-imidazolidinone (IIIB, sertindole). The method can prepare the sertindole and a structuralanalog thereof with high selectivity and high yield, the purity of the prepared sertindole is over 99.5 percent, and the yield can reach 85 to 90 percent. The method is simple and convenient to operate, has an easily controllable reaction condition and high selectivity, is environment-friendly, and is suitable for industrial production.

The invention provides an organochlorine content determination method. The method comprises the following steps: weighing a pure chlorohydrocarbon compound contained in chemical engineering products, and diluting by using a solvent to form a certain concentration of a solution, wherein the solvent can be one or more of water, N,N-dimethyl formamide, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolone and liquid paraffin; and respectively adding standard solutions into sample bottles, sealing by using a sealer, putting the sample bottles in a headspace sample cell, setting gas chromatographic operation parameters, and testing by adopting a gas chromatographic static headspace technology. The method for determining the content of organochlorine in the chemical engineering products by using gas chromatography has the advantages of high sensitivity, simple operation, and elimination of test errors brought by manual operation due to the adoption of the static headspace technology.

The invention relates to a preparation technology of mezlocillin sodium, and belongs to the technical field of drug synthesis. The preparation technology comprises the steps of performing an acylation reaction on ampicillin trihydrate and 1-chloroformyl-3-mesyl-2-imidazolidinone under a low-temperature alkaline condition, performing decoloration, filtering, acidification, washing and dehydration, adding sodium salt, and then performing crystallization to obtain mezlocillin sodium, wherein ampicillin needs to be dissolved and clarified by triethylamine prior to the acylation reaction; and 1-chloroformyl-3-mesyl-2-imidazolidinone and an ethyl acetate solvent are mixed and then added to a reaction system twice. According to the preparation technology, a dissolution manner of ampicillin trihydrate is changed and an addition manner of 1-chloroformyl-3-mesyl-2-imidazolidinone is changed, so that a side reaction in a reaction process is reduced; the washing is performed by purified water after the acidification and anhydrous sodium acetate is used during the crystallization, so that impurities are further reduced; compared with an original drug, a prepared product has the advantages in the quantity and levels of the impurities.

Disclosed is an emulsifiable concentrate composition characterized by containing not less than 0.5% by weight but not more than 25% by weight of a hydrophobic agrochemically active compound, not less than 5% by weight but not more than 15% by weight of a surfactant, not less than 2% by weight but not more than 60% by weight of an aromatic hydrocarbon solvent, not less than 2% by weight but not more than 60% by weight of an ether compound represented by the following formula (1): R¹—O-A¹-O-A²-(O-A³)_n—O—R² (wherein R¹ and R² respectively represent a C₁-C₃ alkyl group; A¹, A² and A³ respectively represent an ethylene group or a propylene group; and n represents 0, 1 or 2), and not less than 12% by weight but not more than 90% by weight of 1,3-dimethyl-2-imidazolidinone. The emulsifiable concentrate composition is also characterized in that the weight ratio of 1,3-dimethyl-2-imidazolidinone to the ether compound (1,3-dimethyl-2-imidazolidinone:ether compound) is within the range from 1:0.03 to 1:2.

The invention discloses a modified dicyandiamide formaldehyde-mimic enzyme compound sewage treatment agent. The sewage treatment agent is prepared from 20 to 50 parts by mass of a modified dicyandiamide formaldehyde polymer, 1 to 5 parts by mass of ethylene diaminetetraacetic acid tetrasodium salt, 5 to 20 parts by mass of ferrous sulfate heptahydrate, 1 to 3 parts by mass of polyferric sulfate, 1 to 5 parts by mass of calcium sulfate and 2 to 6 parts by mass of aluminum sulfate. A modifier of the modified dicyandiamide formaldehyde polymer is ethylenediamine or N-dihydroxyaniline or 2-imidazolidinone. The invention utilizes combination of a mimic enzyme technology and the modified dicyandiamide formaldehyde to improve the reaction efficiency of oxidation, complexation and polymerization of the mimic enzyme and organic pollutes. The sewage treatment agent realizes stable mimic enzyme catalysis and has good organic pollutants and chroma removal effects and has a low cost.