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Hydrochloric Acid → 2-Chloro-1-phenylethanol, (+)-

HRID 1088202
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1088202
C([O:6][C@@H:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:8][Cl:9])(=O)CCC.Cl>>[Cl:9][CH2:8][C@H:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[OH:6]
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Komponenten

3

Edukt 2

HCID 313Hydrochloric AcidHCID 14288517(S)-2-chloro-1-phenylethyl butyrate

Produkt 1

HCID 6433232-Chloro-1-phenylethanol, (+)-Ausbeute 23 %

Versuchsvorschrift

Sixteen grammes of enzyme (produced by Amano pharmaceutical Co. Ltd., Lipase "Amano CES"), 7.9g (0.05mol) of (R,S)-2-chloro-1-phenylethanol and 17.8g (0.059mol) of tributyrin were charged into three-necked flask and reacted with stirring for 16days at 35° C. After the reaction was stopped, the enzyme was removed by filtration, the filtrate was concentrated by distillation under reduced pressure, and the desired compounds were isolated by column chromatography. As the result, 4.0g of (R)-2-chloro-1-phenylethanol (yield: 50%, 58% ee) and (S)-2-chloro-1-phenylethyl butyrate were obtained. The obtained (S)-2-chloro-1-phenylethyl butyrate was hydrolyzed in an acidic solution of hydro chloric acid, and (S)-2-chloro-1-phenylethanol (yield: 23%, >99% ee) was obtained. Optical purity of the obtained compounds was determined by HPLC of optical resolution.

Quellen und Nachweise

ORD-Eintrag
ord-58c8239059cb4a898f83c7f2d002efee
Quelldatensatz
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04962031

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