2-Chloro-6-methylphenyl isocyanate → N-(2-hydroxy-4-nitrophenyl) N'-(2-chloro 6-methylphenyl)urea
反応式
[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]参加物
3
実験手順
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)+
後処理
- customIt was purified by dilution with methylene chloride and precipitation with hexane
- filtrationFiltering
出典と根拠
- ORDレコード
- ord-53befdedb0c04fa4990f564b30cc60a7
- 出典データセット
- uspto-grants-1998_07
- 特許番号
- US05780483
反応ノート
読み込み中…