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1,2-Dichlorobenzene → HCID 15029656, 화합물

HRID 1607247
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반응식

HRID 1607247 반응식
[CH3:1][O:2][C:3]1[CH:25]=[CH:24][C:6]([C:7]([C:9]2[O:10][C:11]3[CH:18]=[CH:17][C:16]([Cl:19])=[C:15]([O:20]CC=C)[C:12]=3[C:13]=2[CH3:14])=[O:8])=[CH:5][CH:4]=1.Cl[C:27]1[CH:32]=CC=C[C:28]=1Cl>>[CH3:1][O:2][C:3]1[CH:25]=[CH:24][C:6]([C:7]([C:9]2[O:10][C:11]3[C:18]([CH2:32][CH:27]=[CH2:28])=[CH:17][C:16]([Cl:19])=[C:15]([OH:20])[C:12]=3[C:13]=2[CH3:14])=[O:8])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 72391,2-DichlorobenzeneHCID 15029655HCID 15029655, 화합물

생성물 1

HCID 15029656HCID 15029656, 화합물수율 27%

실험 절차

A mixture of 2-(p-methoxybenzoyl)-3-methyl-4-allyloxy-5-chlorobenzofuran (400 mg; 1.12mmoles) in ortho-dichlorobenzene (15 mL) was refluxed under nitrogen for 1.5 hours. The reaction mixture was cooled to room temperature and purified by chromatography on silica gel using 20% ethylacetate as eluent to yield 110 mg (27%) of 2-(p-methoxybenzoyl)-3-methyl-4-hydroxy-5-chloro-7-allylbenzofuran.

후처리

  1. temperaturewas refluxed under nitrogen for 1.5 hours
  2. custompurified by chromatography on silica gel using 20% ethylacetate as eluent

출처 및 근거

ORD 기록
ord-af10cc9da37a4af1b6cc3659bc4ada28
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04863958

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