1966•Bulletin of the Chemical Society of JapanRequires access

Studies of C-Substituted Tartaric Acid. I. The Preparation of Optically Active 2-Methyltartaric and 2, 3-Dimethyltartaric Acid

Susumu Tatsumi, Yoshiharu Izumi, Masami Imaida, Yoshio Fukuda, Shiro Akabori

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Abstract

Abstract Two racemic forms of 2-methyltartaric acid were prepared, and their optical resolutions were performed. Four optically active isomers were obtained. 2, 3-Dimethyltartaric acid was also prepared and separated into two isomeric optically inactive forms. The isomer with the higher melting point could be resolved into two optically active isomers, but the other, with the lower melting point, could not. The former was, therefore, assigned to the racemic configuration, and the latter, to the meso configuration.

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Abstract Two racemic forms of 2-methyltartaric acid were prepared, and their optical resolutions were performed. Four optically active isomers were obtained. 2, 3-Dimethyltartaric acid was also prepared and separated into two isomeric optically inactive forms. The isomer with the higher melting point could be resolved into two optically active isomers, but the other, with the lower melting point, could not. The former was, therefore, assigned to the racemic configuration, and the latter, to the meso configuration.

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Available abstract

Abstract Two racemic forms of 2-methyltartaric acid were prepared, and their optical resolutions were performed. Four optically active isomers were obtained. 2, 3-Dimethyltartaric acid was also prepared and separated into two isomeric optically inactive forms. The isomer with the higher melting point could be resolved into two optically active isomers, but the other, with the lower melting point, could not. The former was, therefore, assigned to the racemic configuration, and the latter, to the meso configuration.

Key concepts: Chemistry, Optically active, Tartaric acid, Organic chemistry, Stereochemistry, Citric acid

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