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Acetic Anhydride → HCID 23248656, 화합물

HRID 1830796
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인쇄 미리보기

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HRID 1830796 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-0dd5cb84192341dc84bd928f2a81474b
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067531B2

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