Abstract:
Crystals of an aromatic 0,0'-diacyltartaric acid of the formula (VIII): wherein R and R are the same as or different from one another and each is a hydrogen atom, halogen atom or C1 - C4 alkyl group are sufficiently uniform in size that 95% to 98% of them pass through a 20-mesh sieve. Such crystals may be prepared by hydrolyzing an aromatic carboxylic anhydride of the formula (IV): wherein R and R are as defined above, to form the corresponding acid (VIII) in the form of an oil and crystallizing the acid in the presence of an organic solvent which is immiscible with water to form crystals of the hydrate of the acid (VIII). For the crystallization process, each of the organic solvent immiscible with water and seed crystals of the acid (VIII) are added to the oil of the acid (VIII) present in the reaction mixture.
Abstract:
Crystals of an aromatic 0,0'-diacyltartaric acid of the formula (VIII): wherein R and R are the same as or different from one another and each is a hydrogen atom, halogen atom or C1 - C4 alkyl group are sufficiently uniform in size that 95% to 98% of them pass through a 20-mesh sieve. Such crystals may be prepared by hydrolyzing an aromatic carboxylic anhydride of the formula (IV): wherein R and R are as defined above, to form the corresponding acid (VIII) in the form of an oil and crystallizing the acid in the presence of an organic solvent which is immiscible with water to form crystals of the hydrate of the acid (VIII). For the crystallization process, each of the organic solvent immiscible with water and seed crystals of the acid (VIII) are added to the oil of the acid (VIII) present in the reaction mixture.
Abstract:
Crystals of an aromatic 0,0'-diacyltartaric acid of the formula (VIII): wherein R and R are the same as or different from one another and each is a hydrogen atom, halogen atom or C1 - C4 alkyl group are sufficiently uniform in size that 95% to 98% of them pass through a 20-mesh sieve. Such crystals may be prepared by hydrolyzing an aromatic carboxylic anhydride of the formula (IV): wherein R and R are as defined above, to form the corresponding acid (VIII) in the form of an oil and crystallizing the acid in the presence of an organic solvent which is immiscible with water to form crystals of the hydrate of the acid (VIII). For the crystallization process, each of the organic solvent immiscible with water and seed crystals of the acid (VIII) are added to the oil of the acid (VIII) present in the reaction mixture.
Abstract:
Crystals of an aromatic 0,0'-diacyltartaric acid of the formula (VIII): wherein R and R are the same as or different from one another and each is a hydrogen atom, halogen atom or C1 - C4 alkyl group are sufficiently uniform in size that 95% to 98% of them pass through a 20-mesh sieve. Such crystals may be prepared by hydrolyzing an aromatic carboxylic anhydride of the formula (IV): wherein R and R are as defined above, to form the corresponding acid (VIII) in the form of an oil and crystallizing the acid in the presence of an organic solvent which is immiscible with water to form crystals of the hydrate of the acid (VIII). For the crystallization process, each of the organic solvent immiscible with water and seed crystals of the acid (VIII) are added to the oil of the acid (VIII) present in the reaction mixture.
Abstract:
A process for preparing optically active piperazinecarboxylic acid derivatives by the resolution of diastereomeric salts wherein an optically active acidic amino acid derivative is used as the agent for optical resolution to thereby enhance the recovery of the agent and the production efficiency. N-Acyl and N-sulfonyl derivatives of optically active acidic amino acids are usable as the above optically active acidic amino acid derivatives.
Abstract:
PROBLEM TO BE SOLVED: To obtain a highly pure acylpiperazine derivative hydrochloride or sulfonylpiperazine derivative hydrochloride. SOLUTION: When a piperazine derivative is acylated or sulfonylated to produce the acylpiperazine derivative hydrochloride or sulfonylpiperazine derivative hydrochloride, a tertiary amine is added.
Abstract:
PROBLEM TO BE SOLVED: To provide a method for stably storing an aqueous solution of an optically active tartaric acid salt produced by microbial reaction. SOLUTION: The pH of an aqueous solution of an optically active tartaric acid salt is adjusted to
Abstract:
PROBLEM TO BE SOLVED: To obtain an optically active piperidine derivative, especially optically active 3-[3-(methylsulfonyl)phenyl]-1-propylpiperidine or its acid salt with high optical purity in high yield. SOLUTION: The production method of the optically active piperidine derivative, especially optically active 3-[3-(methylsulfonyl)phenyl]-1-propylpiperidine or its acid salt in which an optically active O,O'-diacyltartaric acid is used as an optically resolving reagent.