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HRID 357723作成日:2026年10月26日

Diisopropyl Ether → (R)-2-bromo-1-(3-chlorophenyl)ethanol

https://huagongshe.com/reaction/357723

反応式

関与物質

役割名称HCID仕込み量
反応物Diisopropyl EtherHCID 7914—
反応物Acetic AnhydrideHCID 7918—
反応物2-Bromo-1-(3-chlorophenyl)ethanolHCID 9964694—
生成物(R)-2-bromo-1-(3-chlorophenyl)ethanolHCID 11075396—
生成物(S)-2-bromo-1-(3-chlorophenyl)ethyl acetateHCID 11747860—

反応手順

To 100 mg (0.4 mmol) of 2-bromo-1-(3-chlorophenyl)ethanol were added 30 mg of Lipase QL (available from Meito Sangyo Co., Ltd.) and 40 mg (0.4 mmol) of acetic anhydride. Diisopropyl ether was added to the mixture to make the total volume to 1 ml. The reaction mixture was then allowed to undergo reaction at a temperature of 35° C. for 72 hours. After the termination of the reaction, the enzyme was removed by filtration. The resulting filtrate was then concentrated under reduced pressure. The concentrated solution was analyzed by 1H-NMR. As a result, it was found that (R)-2-bromo-1-(3-chlorophenyl) ethanol and (S)-2-bromo-1-(3-chlorophenyl)ethyl acetate had been produced in a proportion of 2:3. The concentrated solution was then separated by a thin layer silica gel chromatography. As a result, (R)-2-bromo-1-(3-chlorophenyl)ethanol ([α]D20 =-25.6°, C=1.05) and (S)-2-bromo-1-(3-chlorophenyl)ethyl acetate ([α]D20 =+40.4°, C=0.60) were obtained. The optical purity of (R)-2-bromo-1-(3-chlorophenyl)ethanol thus obtained was analyzed by Chiral HPLC. The results were 100% ee.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05841001
出典データセットuspto-grants-1998_11
ORD IDord-f640bfcaaa3b458781a31bff37f1c3b1
出典メモuspto-grants-1998_11