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HRID 357723생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/357723

반응식

참여 물질

역할이름HCID투입량
반응물Diisopropyl EtherHCID 7914—
반응물Acetic AnhydrideHCID 7918—
반응물2-Bromo-1-(3-chlorophenyl)ethanolHCID 9964694—
생성물(R)-2-bromo-1-(3-chlorophenyl)ethanolHCID 11075396—
생성물(S)-2-bromo-1-(3-chlorophenyl)ethyl acetateHCID 11747860—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05841001
출처 데이터셋uspto-grants-1998_11
ORD IDord-f640bfcaaa3b458781a31bff37f1c3b1
출처 메모uspto-grants-1998_11