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HCID 66965255, 화합물 → HCID 66965766, 화합물

HRID 1514973
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인쇄 미리보기

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HRID 1514973 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([NH:9][C:10](=[O:21])[C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([N+:18]([O-])=O)[CH:12]=2)[CH:5]=[CH:6][C:7]=1[CH3:8]>C(O)C.O=[Pt]=O>[NH2:18][C:13]1[CH:12]=[C:11]([CH:16]=[CH:15][C:14]=1[OH:17])[C:10]([NH:9][C:4]1[CH:5]=[CH:6][C:7]([CH3:8])=[C:2]([CH3:1])[CH:3]=1)=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 66965255HCID 66965255, 화합물

생성물 1

HCID 66965766HCID 66965766, 화합물

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

A solution of N-(3,4-dimethyl-phenyl)-4-hydroxy-3-nitrobenzamide (700 mg) in ethanol (50 mL) was hydrogenated over PtO2 at 40 psi for 3 h. The catalyst was filtered through Celite and the filtrate evaporated to give 3-amino-N-(3,4-dimethylphenyl)-4-hydroxy-benzamide as an off-white solid, mp=220-223° C.; MS (m/z) 255 (M−1).

후처리

  1. filtrationThe catalyst was filtered through Celite
  2. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-ba7af0f4002547f3b2ee36e242ec2aae
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222248B2

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