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Acetic Anhydride → HCID 23248656, 화합물

HRID 1294637
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HRID 1294637 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][C:3]=1[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([Cl:17])[CH:12]=1)=[O:10].[C:18](OC(=O)C)(=[O:20])[CH3:19]>C1(C)C=CC=CC=1>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([NH:1][C:18](=[O:20])[CH3:19])=[C:3]([C:9](=[O:10])[C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([Cl:17])[CH:12]=2)[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 182478(2-Amino-5-bromophenyl)(3-chlorophenyl)methanone

생성물 1

HCID 23248656HCID 23248656, 화합물수율 120.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of intermediate 2 (0.328 mol) and acetic acid anhydride (0.656 mol) in toluene (1200 ml) was stirred and refluxed for one night. The mixture was evaporated and the product was used without further purification, yielding 139 g (quant.) of N-[4-bromo-2-(3-chlorobenzoyl)phenyl]-acetamide (intermediate 3).

후처리

  1. temperaturerefluxed for one night
  2. customThe mixture was evaporated
  3. customthe product was used without further purification

출처 및 근거

ORD 기록
ord-afda9417be2f478eaa7efd83f5d44a02
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241777B2

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