C07C33/22

CHIRAL MULTIDENTATE LIGAND, AND APPLICATION THEREOF IN ASYMMETRIC HYDROGENATION
20230124576 · 2023-04-20 ·

Disclosed are a chiral multidentate ligand (I), a preparation, and an application thereof. In this method, compound (M1) is subjected to condensation with compound (M2) followed by amine deprotection in the presence of a deprotection reagent to obtain compound (M4). Compound (1) is subjected to deprotonation by butyl lithium and phosphorization followed by dimethylamino group substitution to produce compound (3). The compound (3) and the compound (M4) are reacted in the presence of triethylamine to produce chiral multidentate ligands.

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CHIRAL MULTIDENTATE LIGAND, AND APPLICATION THEREOF IN ASYMMETRIC HYDROGENATION
20230124576 · 2023-04-20 ·

Disclosed are a chiral multidentate ligand (I), a preparation, and an application thereof. In this method, compound (M1) is subjected to condensation with compound (M2) followed by amine deprotection in the presence of a deprotection reagent to obtain compound (M4). Compound (1) is subjected to deprotonation by butyl lithium and phosphorization followed by dimethylamino group substitution to produce compound (3). The compound (3) and the compound (M4) are reacted in the presence of triethylamine to produce chiral multidentate ligands.

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Additives to remediate DVB cross-linking and insoluble polymer formation in the styrene process
11661496 · 2023-05-30 · ·

A method of reducing the fouling in a process for the production of styrene, the method comprising: introducing an additive into a stream comprising styrene and byproduct divinyl benzene (DVB), wherein the additive comprises: at least one chemical compound comprising one or more functional groups selected from amines, alcohols, amino-alcohols, labile C—C, esters, carbamates, aldehydes, ketones, acids, acetates, benzoates, labile hydrogen, and combinations thereof, and having a boiling point greater than or equal to 170° C. and within 10, 20, 30, 40, 50, or 60° C. of the boiling point of divinyl benzene (DVB) (which is 195° C.), wherein the at least one chemical compound is active to inhibit divinyl benzene (DVB) crosslinking. A system for carrying out the method is also provided.

Additives to remediate DVB cross-linking and insoluble polymer formation in the styrene process
11661496 · 2023-05-30 · ·

A method of reducing the fouling in a process for the production of styrene, the method comprising: introducing an additive into a stream comprising styrene and byproduct divinyl benzene (DVB), wherein the additive comprises: at least one chemical compound comprising one or more functional groups selected from amines, alcohols, amino-alcohols, labile C—C, esters, carbamates, aldehydes, ketones, acids, acetates, benzoates, labile hydrogen, and combinations thereof, and having a boiling point greater than or equal to 170° C. and within 10, 20, 30, 40, 50, or 60° C. of the boiling point of divinyl benzene (DVB) (which is 195° C.), wherein the at least one chemical compound is active to inhibit divinyl benzene (DVB) crosslinking. A system for carrying out the method is also provided.

Continuous flow synthesis of ibuprofen

This disclosure generally relates to methods of making ibuprofen, naproxen, and derivatives thereof. This disclosure also generally relates to compounds made by the disclosed methods. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Continuous flow synthesis of ibuprofen

This disclosure generally relates to methods of making ibuprofen, naproxen, and derivatives thereof. This disclosure also generally relates to compounds made by the disclosed methods. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Dicarbonyl ruthenium and osmium catalysts

The disclosure relates to dicarbonyl complexes of ruthenium and osmium with bi- and tridentate nitrogen and phosphine ligands. The disclosure relates to methods for preparing these complexes and the use of these complexes, isolated or prepared in situ, as catalysts for reduction reactions of ketones and aldehydes both via transfer hydrogenation or hydrogenation with hydrogen.

Dicarbonyl ruthenium and osmium catalysts

The disclosure relates to dicarbonyl complexes of ruthenium and osmium with bi- and tridentate nitrogen and phosphine ligands. The disclosure relates to methods for preparing these complexes and the use of these complexes, isolated or prepared in situ, as catalysts for reduction reactions of ketones and aldehydes both via transfer hydrogenation or hydrogenation with hydrogen.

COMPOSITIONS AND METHODS FOR REDUCTION OF KETONES, ALDEHYDES AND IMINIUMS, AND PRODUCTS PRODUCED THEREBY

A method of producing an alcohol, comprises reducing an aldehyde or a ketone with a hydridosilatrane. The reducing is carried out with an activator.

COMPOSITIONS AND METHODS FOR REDUCTION OF KETONES, ALDEHYDES AND IMINIUMS, AND PRODUCTS PRODUCED THEREBY

A method of producing an alcohol, comprises reducing an aldehyde or a ketone with a hydridosilatrane. The reducing is carried out with an activator.