4-Bromoaniline → N-(3-cyanophenyl)-N'-(4-bromophenyl)urea
反応式
[C:1]([C:3]1[CH:4]=[C:5]([N:9]=[C:10]=[O:11])[CH:6]=[CH:7][CH:8]=1)#[N:2].[Br:12][C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[CH:15][CH:14]=1.O1CCCC1>C(Cl)(Cl)Cl>[C:1]([C:3]1[CH:4]=[C:5]([NH:9][C:10]([NH:17][C:16]2[CH:18]=[CH:19][C:13]([Br:12])=[CH:14][CH:15]=2)=[O:11])[CH:6]=[CH:7][CH:8]=1)#[N:2]参加物
5
実験手順
A mixture of 3-cyanophenyl isocyanate (3.76 g, 26.1 mmol) and 4-bromoaniline (4.5 g, 26.1 mmol) in 1:1 tetrahydrofuran:chloroform (100 mL). After 72 h at ambient temperature, product was isolated by filtration, the filtrate was washed with cold chloroform and air dried to give 6.6 g of N-(3-cyanophenyl)-N′-(4-bromophenyl)urea (21 mmol).
後処理
- customproduct was isolated by filtration
- washthe filtrate was washed with cold chloroform and air
- customdried
出典と根拠
- ORDレコード
- ord-8181b82618894f04998a9cbf8dcd1e4c
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06521614B1
反応ノート
読み込み中…