C07C53/19

Processes to produce brivaracetam

The present invention provides a scalable synthesis of enantiomerically pure brivaracetam, and related derivatives.

Processes to produce brivaracetam

The present invention provides a scalable synthesis of enantiomerically pure brivaracetam, and related derivatives.

Process or producing polyhydroxyalkanoates from precursors obtained by anaerobic fermentation from fermentable biomass
09650469 · 2017-05-16 · ·

The process for producing polyhydroxyalkanoates or PHA from volatile fatty acid (VFA) molecules, referred to as precursors, produced by anaerobic fermentation from fermentable biomass, characterized in that it comprises at least the following steps: a) extracting the volatile fatty acid (VFA) molecules, without stopping the fermentation, via an extraction means chosen from means that are, at least, insoluble in the fermentation medium, b) collecting, outside the fermentation reactor, the volatile fatty acid (VFA) molecules once they have been extracted, c) synthesizing, by halogenation, using a type of volatile fatty acid (VFA) chosen from the volatile fatty acids collected in step b) and defined according to the desired type of PHA, a given -halo acid, d) synthesizing from this -halo acid molecules of a given -hydroxy acid by reaction with a base, e) polymerizing using the -hydroxy acid obtained a defined polyhydroxyalkanoate (PHA).

Process or producing polyhydroxyalkanoates from precursors obtained by anaerobic fermentation from fermentable biomass
09650469 · 2017-05-16 · ·

The process for producing polyhydroxyalkanoates or PHA from volatile fatty acid (VFA) molecules, referred to as precursors, produced by anaerobic fermentation from fermentable biomass, characterized in that it comprises at least the following steps: a) extracting the volatile fatty acid (VFA) molecules, without stopping the fermentation, via an extraction means chosen from means that are, at least, insoluble in the fermentation medium, b) collecting, outside the fermentation reactor, the volatile fatty acid (VFA) molecules once they have been extracted, c) synthesizing, by halogenation, using a type of volatile fatty acid (VFA) chosen from the volatile fatty acids collected in step b) and defined according to the desired type of PHA, a given -halo acid, d) synthesizing from this -halo acid molecules of a given -hydroxy acid by reaction with a base, e) polymerizing using the -hydroxy acid obtained a defined polyhydroxyalkanoate (PHA).

METHOD FOR PRODUCING CARBOXYLIC ACID ANHYDRIDE AND METHOD FOR PRODUCING CARBOXYLIC ACID ESTER
20170088502 · 2017-03-30 · ·

Provided is a production method whereby corresponding carboxylic acid anhydrides and carboxylic acid esters can be obtained at high yield from various carboxylic acids even without a solvent and near room temperature. A method for producing a carboxylic acid anhydride represented by formula (II), the method comprising reacting a compound represented by formula (I) and a carboxylic acid in the presence of a Group II metal compound having an ionic ligand containing an oxygen atom. A method for producing a carboxylic acid ester, the method comprising reacting a carboxylic acid anhydride produced by the aforementioned method and an alcohol. In formula (I), R.sup.1 represents a C.sub.1-20 hydrocarbon group. In formula (II), R.sup.2 represents a C.sub.1-20 hydrocarbon group.

METHOD FOR PRODUCING CARBOXYLIC ACID ANHYDRIDE AND METHOD FOR PRODUCING CARBOXYLIC ACID ESTER
20170088502 · 2017-03-30 · ·

Provided is a production method whereby corresponding carboxylic acid anhydrides and carboxylic acid esters can be obtained at high yield from various carboxylic acids even without a solvent and near room temperature. A method for producing a carboxylic acid anhydride represented by formula (II), the method comprising reacting a compound represented by formula (I) and a carboxylic acid in the presence of a Group II metal compound having an ionic ligand containing an oxygen atom. A method for producing a carboxylic acid ester, the method comprising reacting a carboxylic acid anhydride produced by the aforementioned method and an alcohol. In formula (I), R.sup.1 represents a C.sub.1-20 hydrocarbon group. In formula (II), R.sup.2 represents a C.sub.1-20 hydrocarbon group.