Abstract: A sulfonic acid or carboxylic acid containing a carbonyl group, or a salt thereof represented by the following formula: R1—C(?O)—(CR22)n—(OR3)p—(CR42)q-L-A wherein R1, R2, R3, R4, n, p, q, A and L are as defined herein.

Abstract: Disclosed is a method for preparing methyl methacrylate (MMA), the method including: (1) separating isobutene containing saturated hydrocarbon (n-butane and iso-butane), via a catalytic distillation process from a stream of C4 hydrocarbons containing butadiene, n-butene, and isobutene; (2) producing methacrolein via a first oxidation reaction of the separated isobutene; (3) producing methacrylic acid via a second oxidation reaction of the produced methacrolein; and (4) esterifying the produced methacrylic acid with methanol. By having a high heat capacity, the amount of nitrogen added is minimized to reduce the size of the reactor and the amount of gas production at a rear end, which has a high economic feasibility due to the effect of reducing investment and investment cost.

Abstract: Disclosed are a reduction method and reduction product of an alkenyl active methylene compound. The reduction reaction comprises the following steps: taking an alkenyl active methylene compound as a substrate, a metal hydride as a reducing agent, and a palladium compound as a catalyst, performing a reduction reaction to obtain a reduction product, and then reducing the alkenyl active methylene compound. The reduction system is a simple method for reducing the alkenyl active methylene compound, and the used hydride and palladium compound catalyst are both reagents that could easily be obtained in a laboratory. Compared with conventional hydrogen hydrogenation methods and reduction methods of reducing agents, the method is easier to operate, higher in safety, mild in conditions, and high in reaction yield, a reaction in a one-pot two-step manner can be achieved, and high atom economy and step economy can be obtained.

Abstract: A method for producing methyl methacrylate including: a distillation step including: supplying a reaction solution, which is obtained by subjecting methacrolein, methanol, and molecular oxygen to oxidative esterification in an oxidative esterification reactor and which contains the methyl methacrylate as a reaction product, to a first distillation column located at downstream of the oxidative esterification reactor, extracting a fraction containing the methacrolein and the methanol from a medium section of the first distillation column, and extracting a column bottom liquid containing the methyl methacrylate from a column bottom of the first distillation column, wherein a concentration of the methanol in the column bottom liquid is 1% by mass or more and 30% by mass or less.

Abstract: A process is described for the preparation of polyglycerol fatty acid esters from a reaction mixture to which a metallic catalyst is added, as well as to a method for the purification of an intermediate synthesis product which contains excess fatty acid in addition to polyglycerol fatty acid esters. Compared with the prior art, a significantly improved yield and a higher process speed is obtained along with more economic use of raw materials, auxiliary materials, solvents and energy.

Abstract: Embodiments of the present disclosure generally relate to processes for converting disulfides to conversion products and to processes for producing cysteic acid. In an embodiment, a process for converting cystine to a conversion product is provided. The process include introducing an organic peroxide and water to cystine to form a mixture. The process further includes reacting the mixture, under conversion conditions, to form the conversion product, wherein the conversion product comprises cysteic acid, an amount of cysteic acid in the conversion product is greater than about 90 wt % based on a total weight of the conversion product, and the conversion conditions comprise a conversion temperature from about 15° C. to about 50° C. The process further includes heating the conversion product to remove the organic peroxide.

Abstract: A method of recovering an organic acid from an aqueous solution may include extracting the organic acid dissolved in the aqueous solution into a water immiscible extraction phase. The water immiscible extraction phase has an extractant for the organic acid. The method may also include separating the extraction phase from the aqueous solution, adding an alcohol to the extraction phase separated from the aqueous solution, and forming an ester from the organic acid and the alcohol.

Abstract: A method for preparing a ?-amino phosphonic acid derivative includes: dissolving N-(arylvinyl)benzamide, dialkyl phosphite, manganese acetate, and potassium carbonate in a solvent and reacting at room temperature to obtain (2-benzamido-1-arylvinyl)dialkyl-phosphonate derivative; and hydrolyzing (2-benzamido-1-arylethyl)dialkylphosphonate derivative to obtain ?-amino phosphonic acid derivative. The N-(arylvinyl)benzamide derivative is used as starting material. The raw materials are easy to obtain and are of many different types. A method of preparing ?-aminophosphonic acid derivative includes: dissolving N-(arylvinyl)benzamide, dialkyl phosphite, manganese acetate and potassium carbonate in a solvent, reacting at room temperature to obtain (2-benzamide-1-arylvinyl) dialkyl phosphonate derivative, and then reducing and hydrolyzing the compound to obtain ?-aminophosphonic acid derivative.

Abstract: A difunctional biphenyl compounds corresponding to formula (I) wherein Alk, Alk? and R are as defined in the description. These compounds are suitable as hardeners for thermosetting resins, especially epoxy resins.

Abstract: The present invention relates to a scalable process for the making of elagolix, its salts and the process of intermediate compounds.

Abstract: The present disclosure relates to granules comprising an L-amino acid and a method for preparing the same. The method may comprise: (a) preparing a fermentation liquid of L-amino acid; (b) removing moisture from the fermentation liquid of L-amino acid such that the solid content of the fermentation liquid of L-amino acid is in a range of 20% to 90%; (c) forming granulated particles with a moisture content of 0% to 40% by mixing the concentrated fermentation liquid of L-amino acid with a seed; (d) drying the granulated particles formed in Step (c); (e) sieving the granulated particles dried in Step (d); and (f) pulverizing or circulating the particles left in step (e) to be recycled as the seed in step (c).

Abstract: An object of the present invention is to provide a non-solvate crystal of eucomic acid having a low methanol content and excellent fluidity, and a method for producing the same. The present invention can provide a non-solvate crystal of eucomic acid having a low methanol content and excellent fluidity by drying a methanol solvate crystal of eucomic acid.

Abstract: The invention relates to a method for operating a production plant for producing a chemical product (1) by reacting a H-functional reactant (2) with phosgene (3) during an interruption in production when taking at least one plant part of the production plant out of operation, wherein low-oxygen and oxygen-rich phosgene-containing exhaust gas flows are directed separately from one another in different phosgene decomposition directions and separately from one another—at spatially different points—into a combustion device, wherein plant parts that have not been taken out of operation are operated in a closed-circuit operating mode. The invention also relates to a production plant for producing a chemical product by reacting H-functional reactants with phosgene, which is suitable for being operated with the method according to the invention.

Abstract: The invention relates to a process for preparing an ester by alkoxycarbonylation of a C2 to C20 hydrocarbon having at least one multiple bond, preferably having at least one olefinic double bond, in which the homogeneous catalyst system used is separated from the product mixture by means of membrane separation and recycled into the reaction zone. In a development of the present invention, the ester thus formed is converted into another ester by transesterification.

Abstract: The method for producing pentamethylene diisocyanate includes a reaction step, in which carbonyl chloride is allowed to react with pentamethylenediamine to produce a reaction mixture containing pentamethylene diisocyanate and a tar component containing a chlorine-containing component; a heating step, in which the reaction mixture is heated; and a purification step, in which the reaction mixture after the heating step is purified to separate the pentamethylene diisocyanate from the tar component, wherein in the heating step, the reaction mixture is heated without removing the tar component from the reaction mixture.

Abstract: A leuco compound comprises an antioxidant moiety covalently bonded to a leuco moiety. A laundry care composition comprises (a) at least one laundry care ingredient and (b) a leuco compound as described above. A method of treating a textile comprises the steps of (a) providing such a laundry care composition; (b) adding the laundry care composition to a liquid medium; (c) placing textile articles in the liquid medium; (d) optionally, rinsing the textile; and (e) drying the textile articles.

Abstract: Described herein is a process for the preparation of a mixture of compounds of formula having a weight ratio of the cis-diastereomers to trans-diastereoisomers higher than 1:1, where R1 represents a C1-8 alkyl group, a C2-8 alkenyl group or a C2-8 alkynyl group, each optionally substituted with one or two of a C1-4 alkyl alkoxy ether group and/or a C1-4 alkyl carboxylester group and R2 represents a C1-6 alkyl, a C2-6 alkenyl or a C2-6 alkynyl group, each optionally substituted with a C1-4 alkyl alkoxy ether group, a carboxylic acid group or a C1-4 alkyl carboxylester group and compounds suitable in the process.

Abstract: In the embodiments, an aqueous hydrochloric acid solution instead of hydrogen chloride gas and solid triphosgene instead of phosgene gas may be used in the process of preparing a diisocyanate from a diamine through a diamine hydrochloride. In addition, the embodiments provide processes for preparing a diisocyanate composition and an optical lens, which are excellent in yield and quality with mitigated environmental problems by controlling the size of the diamine hydrochloride composition, the b* value according to the CIE color coordinate of the diamine hydrochloride composition, or the content of water in the diamine hydrochloride composition within a specific range.

Abstract: The present technology provides a process for selectively preparing an (E)-(2-(chloromethyl)-3-fluoroallyl)carbamate compound by refluxing an (E/Z)-(2-(chloromethyl)-3-fluoroallyl)carbamate compound in an organic solvent, followed by crystallization by cooling.

Abstract: Described herein is an improved conversion of nitrous oxide (N2O) present as a by-product in a chemical process to NOx which can be further converted to a useful compound or material, such as nitric acid.