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2-Chloro-1-(2,5-dimethoxyphenyl)ethanone → 2-Chloro-1-(3,4-dimethoxyphenyl)ethan-1-ol

HRID 258228
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인쇄 미리보기

반응식

HRID 258228 반응식
ClCC(C1C=C(OC)C=CC=1OC)=O.[Cl:15][CH2:16][C:17]([C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=1)=[O:18].ClCC(C1C=C(OC)C=CC=1OC)O>>[Cl:15][CH2:16][CH:17]([C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=1)[OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 2736162-Chloro-1-(2,5-dimethoxyphenyl)ethanoneHCID 122925932-Chloro-1-(3,4-dimethoxyphenyl)ethanoneHCID 232071012-Chloro-1-(2,5-dimethoxyphenyl)ethan-1-ol

생성물 1

HCID 142885082-Chloro-1-(3,4-dimethoxyphenyl)ethan-1-ol

실험 절차

Cultivation, reaction and purification were carried out in the same way as described in Example 9 except that 2-chloro-1-(2',5'-dimethoxyphenyl) ethanone, 2-chloro-1-(3',4'-dimethoxyphenyl) ethanone were used as substrate and (-)-2-chloro-1-(2',5'-dimethoxyphenyl) ethanol, (-)-2-chloro-1-(3',4'-dimethoxyphenyl) ethanol were obtained. The yield, specific rotation and optical purity determined by high-performance liquid chromatography were shown in Table 10.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customCultivation, reaction and purification

출처 및 근거

ORD 기록
ord-9a8007b831c549f9b125be1efb6d57c8
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05266485

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