C07C51/573

Process for the manufacture of carboxylic anhydride

The present invention concerns a process for manufacturing a fraction comprising carboxylic acid anhydride by reaction of a fraction comprising carboxylic acid with a ketene, and the use of the fraction comprising carboxylic acid anhydride in a process for acylation of polysaccharides.

Process for the manufacture of carboxylic anhydride

The present invention concerns a process for manufacturing a fraction comprising carboxylic acid anhydride by reaction of a fraction comprising carboxylic acid with a ketene, and the use of the fraction comprising carboxylic acid anhydride in a process for acylation of polysaccharides.

Synthesis of (meth) acrylic anhydride by transanhydrization

The invention relates to a method for producing a (meth)acrylic anhydride A-C(O)O(O)C-A, comprising the following steps: a) a step of reacting an anhydride BC(O)O(O)CB with an acid A-COOH, resulting in the formation of mixed anhydride A-C(O)O(O)CB and acid BCOOH; and b) a step of reacting the mixed anhydride with A-COOH, resulting in the (meth)acrylic anhydride. According to the invention, reaction steps (a) and (b) are carried out in the presence of hydrated triflic acid, and the anhydride A-C(O)O(O)C-A is isolated from the reaction medium produced in step (b) as follows: e1) heavy compounds having a volatility less than or equal to that of the anhydride A-C(O)O(O)C-A are separated from the reaction medium, said compounds including the anhydride and the hydrated triflic acid; e2) the anhydride is separated from the heavy compounds by difference in volatility.

Synthesis of (meth) acrylic anhydride by transanhydrization

The invention relates to a method for producing a (meth)acrylic anhydride A-C(O)O(O)C-A, comprising the following steps: a) a step of reacting an anhydride BC(O)O(O)CB with an acid A-COOH, resulting in the formation of mixed anhydride A-C(O)O(O)CB and acid BCOOH; and b) a step of reacting the mixed anhydride with A-COOH, resulting in the (meth)acrylic anhydride. According to the invention, reaction steps (a) and (b) are carried out in the presence of hydrated triflic acid, and the anhydride A-C(O)O(O)C-A is isolated from the reaction medium produced in step (b) as follows: e1) heavy compounds having a volatility less than or equal to that of the anhydride A-C(O)O(O)C-A are separated from the reaction medium, said compounds including the anhydride and the hydrated triflic acid; e2) the anhydride is separated from the heavy compounds by difference in volatility.

Synthesis of (meth) acrylic anhydride by transanhydrization

The invention relates to a method for producing a (meth)acrylic anhydride A-C(O)O(O)C-A, comprising the following steps: a) a step of reacting an anhydride BC(O)O(O)CB with an acid A-COOH, resulting in the formation of mixed anhydride A-C(O)O(O)CB and acid BCOOH; and b) a step of reacting the mixed anhydride with A-COOH, resulting in the (meth)acrylic anhydride. According to the invention, reaction steps (a) and (b) are carried out in the presence of hydrated triflic acid, and the anhydride A-C(O)O(O)C-A is isolated from the reaction medium produced in step (b) as follows: e1) heavy compounds having a volatility less than or equal to that of the anhydride A-C(O)O(O)C-A are separated from the reaction medium, said compounds including the anhydride and the hydrated triflic acid; e2) the anhydride is separated from the heavy compounds by difference in volatility.

METHOD FOR PRODUCING ACRYLIC ACID
20240383837 · 2024-11-21 · ·

The present invention provides a method for producing acrylic acid comprising thermally decomposing a poly(3-hydroxypropionate) in the presence of a predetermined transition metal oxide to produce acrylic acid.

Method for separating high-boiling carboxylic acid vinyl ester/carboxylic acid mixtures
09822059 · 2017-11-21 · ·

The invention relates to a method for separating a mixture containing at least one carboxylic acid vinyl ester of general formula RC(O)OCHCH.sub.2 and at least one carboxylic acid of general formula RCOOH, wherein R in either case can be an aliphatic group having 12 to 22 C atoms or a cycloaliphatic group having 12 to 22 C atoms, or an aromatic group having 12 to 22 C atoms, and R can be identical or different, characterized in that the carboxylic acid is converted to its anhydride RC(O)OC(O)R and the carboxylic acid vinyl ester is subsequently separated.

Method for separating high-boiling carboxylic acid vinyl ester/carboxylic acid mixtures
09822059 · 2017-11-21 · ·

The invention relates to a method for separating a mixture containing at least one carboxylic acid vinyl ester of general formula RC(O)OCHCH.sub.2 and at least one carboxylic acid of general formula RCOOH, wherein R in either case can be an aliphatic group having 12 to 22 C atoms or a cycloaliphatic group having 12 to 22 C atoms, or an aromatic group having 12 to 22 C atoms, and R can be identical or different, characterized in that the carboxylic acid is converted to its anhydride RC(O)OC(O)R and the carboxylic acid vinyl ester is subsequently separated.

Method for separating high-boiling carboxylic acid vinyl ester/carboxylic acid mixtures
09822059 · 2017-11-21 · ·

The invention relates to a method for separating a mixture containing at least one carboxylic acid vinyl ester of general formula RC(O)OCHCH.sub.2 and at least one carboxylic acid of general formula RCOOH, wherein R in either case can be an aliphatic group having 12 to 22 C atoms or a cycloaliphatic group having 12 to 22 C atoms, or an aromatic group having 12 to 22 C atoms, and R can be identical or different, characterized in that the carboxylic acid is converted to its anhydride RC(O)OC(O)R and the carboxylic acid vinyl ester is subsequently separated.

Method for preparing levulinic acid using solid acid catalyst in presence of ethylene glycol-based compound solvent derived from biomass

Provided is a method for preparing levulinic acid using a solid acid catalyst in the presence of an ethylene glycol-based compound. The levulinic acid according to the present invention can be prepared by using a linear or cyclic ethylene glycol-based compound as a solvent and preparing the levulinic acid from fructose in the presence of the solid acid catalyst at a reaction temperature of 100 to 200 C., thereby reducing the dependency on petroleum in response to greenhouse gas emission regulations. Also, a high yield of levulinic acid can be obtained from fructose, and the solvent and the catalyst can be efficiently separated, collected, and reused after the reaction has completed.