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2-Chloro-6-methylphenyl isocyanate → N-(2-hydroxy-4-nitrophenyl) N'-(2-chloro 6-methylphenyl)urea

HRID 1385360
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HRID 1385360 반응식
[OH:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:3]=1[NH2:4].[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([CH3:19])[C:14]=1[N:20]=[C:21]=[O:22]>>[OH:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:3]=1[NH:4][C:21]([NH:20][C:14]1[C:15]([CH3:19])=[CH:16][CH:17]=[CH:18][C:13]=1[Cl:12])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 2681232-Chloro-6-methylphenyl isocyanateHCID 49847212-Amino-5-Nitrophenol

생성물 1

HCID 19595671N-(2-hydroxy-4-nitrophenyl) N'-(2-chloro 6-methylphenyl)urea수율 29%

실험 절차

The urea was prepared from 2-hydroxy 4-nitro aniline (500 mg, 3.24 mmol) and 2-chloro 6-methyl phenyl isocyanate by general Method B. It was purified by dilution with methylene chloride and precipitation with hexane. Filtering afforded the desired compound (0.31 g, 29%). EI-MS m/z 322 (M+H)+

후처리

  1. customIt was purified by dilution with methylene chloride and precipitation with hexane
  2. filtrationFiltering

출처 및 근거

ORD 기록
ord-bc4ef0ed63874d1eaa91ae57f2c37462
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06262113B1

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