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

HRID 1088202
ノート
印刷プレビュー

反応式

HRID 1088202 の反応式
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]
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

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

実験手順

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.

出典と根拠

ORDレコード
ord-58c8239059cb4a898f83c7f2d002efee
出典データセット
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04962031

反応ノート

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