Process for producing optically active alcohols

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

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502162, 568875, 568903, C07C 2917, C07C 31125, C07C 31135, C07C 33025

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active

049622420

ABSTRACT:
A process for producing an optically active alcohol represented by formula (I): ##STR1## wherein R.sub.1 is an alkyl group having from 2 to 11 carbon atoms, an alkenyl group having from 3 to 11 carbon atoms, an alkadienyl group having from 6 to 11 carbon atoms, a cyclohexyl group, an cyclohexylmethyl group, or a cyclohexylethyl group, provided that the olefin in the alkenyl group or alkadienyl group is not conjugated to the olefin at the 2-position thereof; and * means an asymmetric carbon atom,
is disclosed, comprising subjecting an olefinic alcohol represented by formula (II): ##STR2## wherein R.sub.1 is the same as defined above to asymmetric hydrogenation in the presence of, as a catalyst, a ruthenium-optically active phosphine complex.
According to the process of the invention, the desired optically active alcohols which are useful not only as intermediates for the manufacture of perfumes and vitamin E but also as liquid crystal materials can be produced with high optical purities.

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Inoue et al., "Asymmetric Hydrogenation of Geraniol, Etc.," Chemistry Letterrs, pp. 1007-1008 (1985).
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Chemistry Letters, No. 7, 1985, pp. 1007-1008, The Chemical Society of Japan, Tokyo, JP; Shin-Ichi Inoue et al: "Asymmetric Hydrogenation of Geraniol and Nerol Catalyzed by BINAP-Rhodium (I) Complexes".

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