2-Chloro-1-(4-methylphenyl)ethan-1-one → 2-Chloro-1-(4-methylphenyl)ethan-1-ol

HRID 258227Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 258227
ClCC(C1C=CC=CC=1C)=O.ClCC(C1C=CC=C(C)C=1)=O.[Cl:23][CH2:24][C:25]([C:27]1[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=1)=[O:26].ClCC(C1C=CC=CC=1C)O.ClCC(C1C=CC=C(C)C=1)O>>[Cl:23][CH2:24][CH:25]([C:27]1[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=1)[OH:26]

Komponenten

6

Versuchsvorschrift

Cultivation, reaction and purification were carried out in the same way as described in Example 9 except that 2-chloro-1-(2'-methylphenyl) ethanone, 2-chloro-1-(3'-methylphenyl) ethanone, 2-chloro-1-(4'-methylphenyl) ethanone were used as substrate, and (-)-2-chloro-1-(2'-methylphenyl) ethanol, (-)-2-chloro-1-(3'-methylphenyl) ethanol, (-)-2-chloro-1-(4'-methylphenyl) ethanol were obtained. The yield, specific rotation and optical purity determined by high-performance liquid chromatography were shown in Table 6.

Aufarbeitung

  1. customCultivation, reaction and purification

Quellen und Nachweise

ORD-Eintrag
ord-ec896a0080ac4289a57f1677af505f47
Quelldatensatz
uspto-grants-1993_11
Patentnummer
US05266485

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