C07C53/128

Synthesis of building blocks and feedstocks for manufacturing renewable polymers

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

Synthesis of building blocks and feedstocks for manufacturing renewable polymers

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

Preparation of rhodium(III)-2-ethylhexanoate

The present invention provides a method for preparing rhodium (III) 2-ethylhexanoate solutions which supplies the reaction product with higher space yield, as well as lower sodium and chloride ion content. An aqueous solution of an alkali salt of 2-ethylhexanoate is thereby initially converted with a rhodium (III) precursor. The rhodium (III) precursor is selected from rhodium (III) chloride solution, rhodium (III) chloride hydrate, and rhodium (III) nitrate. The mixture is heated for several hours. After cooling to room temperature, the rhodium (III) 2-ethylhexanoate formed is extracted from the aqueous solution with an alcohol that is immiscible in water or a carboxylic acid that is immiscible in water, and optionally washed with aqueous mineral acid. The rhodium (III) 2-ethylhexanoate solution obtainable in this way may be used directly as catalyst in hydroformylation reactions.

Preparation of rhodium(III)-2-ethylhexanoate

The present invention provides a method for preparing rhodium (III) 2-ethylhexanoate solutions which supplies the reaction product with higher space yield, as well as lower sodium and chloride ion content. An aqueous solution of an alkali salt of 2-ethylhexanoate is thereby initially converted with a rhodium (III) precursor. The rhodium (III) precursor is selected from rhodium (III) chloride solution, rhodium (III) chloride hydrate, and rhodium (III) nitrate. The mixture is heated for several hours. After cooling to room temperature, the rhodium (III) 2-ethylhexanoate formed is extracted from the aqueous solution with an alcohol that is immiscible in water or a carboxylic acid that is immiscible in water, and optionally washed with aqueous mineral acid. The rhodium (III) 2-ethylhexanoate solution obtainable in this way may be used directly as catalyst in hydroformylation reactions.

Preparation of rhodium(III)-2-ethylhexanoate

The present invention provides a method for preparing rhodium (III) 2-ethylhexanoate solutions which supplies the reaction product with higher space yield, as well as lower sodium and chloride ion content. An aqueous solution of an alkali salt of 2-ethylhexanoate is thereby initially converted with a rhodium (III) precursor. The rhodium (III) precursor is selected from rhodium (III) chloride solution, rhodium (III) chloride hydrate, and rhodium (III) nitrate. The mixture is heated for several hours. After cooling to room temperature, the rhodium (III) 2-ethylhexanoate formed is extracted from the aqueous solution with an alcohol that is immiscible in water or a carboxylic acid that is immiscible in water, and optionally washed with aqueous mineral acid. The rhodium (III) 2-ethylhexanoate solution obtainable in this way may be used directly as catalyst in hydroformylation reactions.

PROCESS FOR THE PRODUCTION OF DIACYL PEROXIDES

Process for the production of a diacyl peroxide involving the reaction of an anhydride with hydrogen peroxide, removal of the formed carboxylic acid, production of an anhydride from said carboxylic acid, and recycling of the anhydride within the process.

PROCESS FOR THE PRODUCTION OF DIACYL PEROXIDES

Process for the production of a diacyl peroxide involving the reaction of an anhydride with hydrogen peroxide, removal of the formed carboxylic acid, production of an anhydride from said carboxylic acid, and recycling of the anhydride within the process.

SYNTHESIS OF BUILDING BLOCKS AND FEEDSTOCKS FOR MANUFACTURING RENEWABLE POLYMERS

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

SYNTHESIS OF BUILDING BLOCKS AND FEEDSTOCKS FOR MANUFACTURING RENEWABLE POLYMERS

Disclosed are methods or processes of synthesizing building blocks and feedstocks for producing a broader range of polymers, including renewable polymers, from renewable resources such as CO.sub.2. In a process of manufacturing a renewable feedstock for polymer production, a CO.sub.2 derived lactone is prepared and processed to form the renewable feedstock. The process may include alkoxycarbonylation of the CO.sub.2 derived lactone to form a diester and hydrogenation of the diester.

ACID ADDITION SALTS OF APOMORPHINE, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME, AND METHODS OF USING THE SAME
20210179561 · 2021-06-17 ·

Acid addition salt of apomorphine glycolate, acid addition salt of apomorphine sulfamate, and acid addition salt of apomorphine isobutyrate salts are disclosed. Also disclosed are pharmaceutical compositions (e.g., unit dosage forms, e.g., films) containing acid addition salt of apomorphine glycolate, acid addition salt of apomorphine sulfamate, or acid addition salt of apomorphine isobutyrate. Further disclosed are methods of use of acid addition salt of apomorphine glycolate, acid addition salt of apomorphine sulfamate, or acid addition salt of apomorphine isobutyrate.