C07C235/06

INTEGRATED METHODS AND SYSTEMS FOR PRODUCING AMIDE AND NITRILE COMPOUNDS

Provided herein are integrated methods and systems for the production of acrylamide and acrylonitrile compounds and other compounds from at least beta-lactones and/or beta-hydroxy amides.

INTEGRATED METHODS AND SYSTEMS FOR PRODUCING AMIDE AND NITRILE COMPOUNDS

Provided herein are integrated methods and systems for the production of acrylamide and acrylonitrile compounds and other compounds from at least beta-lactones and/or beta-hydroxy amides.

A process for preparation of amides and esters of 2-((2-hydroxypropanoyl)oxy)propanoic acid
20220041542 · 2022-02-10 ·

The present invention describes method of preparation of esters or amides of lactyl lactates of general formula I, where Z denotes to group of R—O or RR′—N and R represent alkyl, aryl or H from lactide and the lactide is in contact with a hydrocarbyl alcohol and a hydrolyzable halide in a non-chlorinated organic solvent, or an amine initiated by a hydrolysable halide or hydrogen halide solution or an ammonium hydrohalide, wherein the hydrocarbyl alcohol or amine is either aliphatic or aromatic and containing 1 to 1000 carbon atoms, preferably 1 up to 150 carbon atoms, and optionally one or more, preferably 1 to 5, —CH.sub.2— groups may be replaced by —O— groups.

Structure for annotation

##STR00001##

A process for preparation of amides and esters of 2-((2-hydroxypropanoyl)oxy)propanoic acid
20220041542 · 2022-02-10 ·

The present invention describes method of preparation of esters or amides of lactyl lactates of general formula I, where Z denotes to group of R—O or RR′—N and R represent alkyl, aryl or H from lactide and the lactide is in contact with a hydrocarbyl alcohol and a hydrolyzable halide in a non-chlorinated organic solvent, or an amine initiated by a hydrolysable halide or hydrogen halide solution or an ammonium hydrohalide, wherein the hydrocarbyl alcohol or amine is either aliphatic or aromatic and containing 1 to 1000 carbon atoms, preferably 1 up to 150 carbon atoms, and optionally one or more, preferably 1 to 5, —CH.sub.2— groups may be replaced by —O— groups.

Structure for annotation

##STR00001##

ACETYLSALICYLIC ACID DERIVATIVE AND APPLICATION THEREOF
20210387950 · 2021-12-16 ·

An acetylsalicylic acid derivative and an application thereof. The present disclosure relates to the field of chemical pharmaceuticals, and in particular, to a compound shown in formula (I) or pharmaceutically acceptable salts thereof.

##STR00001##

Hydrocarbon-containing carboxylic acid, hydrocarbon-containing sulfonic acid, hydrocarbon-containing sulfuric acid ester or salt thereof, and surfactant

The invention provides a novel hydrocarbon-containing carboxylic acid, hydrocarbon-containing sulfonic acid, hydrocarbon-containing sulfuric acid ester, or a salt thereof, and a surfactant. Each of them is a compound represented by the following formula (1):
CR.sup.1R.sup.2R.sup.4—CR.sup.3R.sup.5—X-A
wherein R.sup.1 to R.sup.5 are each H or a monovalent substituent; at least one of R.sup.1 or R.sup.3 is a group represented by the formula: —Y—R.sup.6; at least one of R.sup.2 or R.sup.5 is a group represented by the formula: —X-A or a group represented by the formula: —Y—R.sup.6; and As at the respective appearances are the same as or different from each other, and are each —COOM, —SO.sub.3M, or —OSO.sub.3M.

Hydrocarbon-containing carboxylic acid, hydrocarbon-containing sulfonic acid, hydrocarbon-containing sulfuric acid ester or salt thereof, and surfactant

The invention provides a novel hydrocarbon-containing carboxylic acid, hydrocarbon-containing sulfonic acid, hydrocarbon-containing sulfuric acid ester, or a salt thereof, and a surfactant. Each of them is a compound represented by the following formula (1):
CR.sup.1R.sup.2R.sup.4—CR.sup.3R.sup.5—X-A
wherein R.sup.1 to R.sup.5 are each H or a monovalent substituent; at least one of R.sup.1 or R.sup.3 is a group represented by the formula: —Y—R.sup.6; at least one of R.sup.2 or R.sup.5 is a group represented by the formula: —X-A or a group represented by the formula: —Y—R.sup.6; and As at the respective appearances are the same as or different from each other, and are each —COOM, —SO.sub.3M, or —OSO.sub.3M.

Method of preparing (3R,4S)-3-acetamido-4-allyl-n-(tert-butyl)pyrrolidine-3-carboxamide

A method is provided to conveniently separate racemic (3R,4S)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide and (3S,4R)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide using selective crystallization with chiral carboxylic acids.

Method of preparing (3R,4S)-3-acetamido-4-allyl-n-(tert-butyl)pyrrolidine-3-carboxamide

A method is provided to conveniently separate racemic (3R,4S)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide and (3S,4R)-3-acetamido-4-allyl-N-(tert-butyl)pyrrolidine-3-carboxamide using selective crystallization with chiral carboxylic acids.

Surface primer compositions and methods of use
11352512 · 2022-06-07 · ·

In one embodiment, the present application discloses a surface binding compound of the Formula I or Formula II: ##STR00001##
wherein the variables EG, EG1, SP1, SP2, SP3, Ar and BG are as defined herein. In another embodiment, the application discloses a method for forming a coating on a surface of a substrate using the surface binding compound of the Formula I or Formula II.