Process for the preparation of an optically pure aminoalcohol

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

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549419, 558 52, 558369, 558406, 564184, 564355, 564356, C07D21158, C07C25330, C07C25541, C07C21300

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active

055126804

ABSTRACT:
A process is described for the preparation of (+)-2-(3,4-dichlorophenyl)-4-hydroxybutylamine (I) by reaction of 3,4-dichlorophenylacetonitrile (II) with an alkali metal halogenoacetate, treatment of the 3-cyano-3-(3,4-dichlorophenyl)propionic acid (III) with D-(-)-N-methylglucamine, with second-order asymmetric conversion, hydrolysis of the D-(-)-N-methylglucamine salt of (-)-3-cyano-3-(3,4-dichlorophenyl)propionic acid and enantioconservative reduction of the resulting levorotatory cyanoacid with a borane.

REFERENCES:
patent: 5236921 (1993-08-01), Emonds-Ai et al.
patent: 5317020 (1994-05-01), Emonds-Alt et al.
C.A.; Bastian et. al., 78(1973), 78: 159422w.

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