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N-Benzoyl-3-(trifluoromethyl)-4-nitroaniline → N-[4-amino-3-(trifluoromethyl)phenyl]benzamide

HRID 2233232
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인쇄 미리보기

반응식

HRID 2233232 반응식
[C:1]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[C:12]([C:19]([F:22])([F:21])[F:20])[CH:11]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)C.[Pt](=O)=O>[C:1]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[C:12]([C:19]([F:20])([F:21])[F:22])[CH:11]=1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 44203033N-Benzoyl-3-(trifluoromethyl)-4-nitroaniline

생성물 1

HCID 16772080N-[4-amino-3-(trifluoromethyl)phenyl]benzamide수율 91%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

Platinum dioxide (100 mg, 0.44 mmol) was added to a solution of N-benzoyl 3-(trifluoromethyl)-4-nitroaniline (913 mg, 2.94 mmol) in ethanol (50 ml) at ambient temperature and the reaction stirred for 1.5 hours under an atmosphere of hydrogen. Filtration of the reaction through a pad of celite and solvent evaporation in vacuo, yielded N-benzoyl 3-(trifluoromethyl)-4-aminoaniline (750 mg, 91% yield) as an off-white solid:

후처리

  1. filtrationFiltration of the reaction
  2. customthrough a pad of celite and solvent evaporation in vacuo

출처 및 근거

ORD 기록
ord-6640c2581dca4f0fb5b913abb099c106
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709479B1

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