Abstract:
A METHOD FOR CONVERTING A KETOXIME TO AN N-SUBSTITUTED AMIDE BY REACTING A KETOXIME WITH A COMPLEX OF AN NSUBSTITUTED CARBOXYLIC ACID AMIDE AND SULFUR TRIOXIDE TO FORM A NOVEL COMPOUND OF THE KETOXIME, CARBOXYLIC ACID AMIDE AND SULFUR TRIOXIDE AND DECOMPOSING THIS COMPOUND TO PRODUCE AN N-SUBSTITUTED AMIDE CORRESPONDING TO THE KETOXIME. CYCLOHEXANONE OXIME IS CONVERTED TO CAPROLACTAM.
Abstract:
A HIGH PURITY W-LAUROLACTAM IS PREPARED FROM A CRUDE CYCLODODECANONE OXIME CONTAINING 5% BY WEIGHT OR LESS OF CYCLODODECANONE BY SUBJECTING THE OXIME TO THE BECKMANN REARRANGEMENT REACTION IN THE PRESENCE OF SULFURIC ACID HAVING A CONCENTRATION OF 98% BY WEIGHT OR MORE OR FUMING SULFURIC ACID CONTAINING 20% BY WEIGHT OR LESS OF SULFURIC-ANHYDRIDE, SEPARATING THE THUS FORMED W-LAUROLACTAM FROM THE REACTION MIXTURE, DISSOLVING THE RESULTING W-LAUROLACTAM N A LIQUID AROMATIC HYDROCARBON, WASHING THE SOLUTION WITH AN ALKALI SOLUTION AT A TEMPERATURE OF 60* TO 120* C., AND RECOVERING W-LAUROLACTAM.
Abstract:
A PROCESS FOR PRODUCING E-CAPROLACTAM AND O-ACETYLCYCLOHEXANONE OXIME COMPRISING REACTING 0.01 TO 100 MOLS OF CYCLOHEXANONE OXIME WITH ONE MOL OF N-ACETYLCAPROLACTAM AT A TEMPERATURE OF 30 TO 120*C. FOR 10 MINUTES TO 100 HOURS IN THE PRESENCE OF AN AORGANIC SOLVENT IN AN AMOUNT OF 0 TO 20 TIMES THE TOTAL WEIGHT OF N-ACETYLCAPROLACTAM AND CYCLOHEXANONE OXIME.
Abstract:
Provided are a method of preparing laurolactam including: a) synthesizing laurolactam by Bechmann rearrangement of cyclododecanone oxime under a catalyst system, b) mixing the laurolactam synthesized in a) with a good solvent and removing the catalyst system, and c) mixing the laurolactam from which the catalyst system has been removed in b) with a poor solvent and performing recrystallization, a synthesis device thereof, a laurolactam composition prepared therefrom, and a method of preparing polylaurolactam using the laurolactam composition.
Abstract:
The present invention relates to a laurolactam preparation method and synthesis apparatus, and epoxidation and a rearrangement reaction are performed in the conversion of cyclododecene into cyclododecanone so that the preparation method can synthesize laurolactam having a higher purity with a higher selectivity and in a higher yield than a conventional preparation method.
Abstract:
The present disclosure discloses a MFI topological structure silicon molecular sieve, a preparation method thereof and a catalyst containing the MFI topological structure silicon molecular sieve, wherein the molecular sieve containing a silicon element, an oxygen element and a metallic element, the ions of said metallic element have a Lewis acid characteristic; the content of the metallic element in the molecular sieve is within a range of 5-100 μg/g based on the total amount of the molecular sieve; the BET specific surface area of the molecular sieve is within a range of 400-500 m2/g.
Abstract:
Disclosed herein is an efficient, economical, industrially advantageous, straight-through process for the preparation of cyclic amides, also referred as lactams, in substantially pure form and high yield, from the corresponding cyclic ketones and a hydroxylammonium salt, using a combination of amphoteric metal oxide or amphoteric masked metal oxide and a base.
Abstract:
The present invention relates to a compound represented by formula (I): and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing diabetes, hyperlipidemia, obesity, inflammation related disorders, and related diseases and conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR120. Pharmaceutical compositions and methods of treatment are also included.
Abstract:
Provided is a method for producing an oxime compound with satisfactory selectivity. Provide is a method for producing an oxime represented by the following formula (II): wherein R1 and R2 are respectively the same as defined below, the method including oxidizing an amine represented by the following formula (I): wherein R1 and R2 each independently represents a hydrogen atom, an optionally substituted hydrocarbon group, or an optionally substituted heterocyclic group (provided that R1 and R2 are not simultaneously hydrogen atoms), orR1 and R2, together with the carbon atom to which R1 and R2 are attached, form an optionally substituted alicyclic hydrocarbon group having 3 to 12 carbon atoms [hereinafter sometimes referred to as the amine compound (I)],with oxygen in the presence of a layered silicate.