Cyanogen Bromide → 2-Chloro-5-ethylphenylcyanamide
反応式
[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([CH2:9][CH3:10])=[CH:5][C:3]=1[NH2:4].Br[C:12]#[N:13]>O>[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([CH2:9][CH3:10])=[CH:5][C:3]=1[NH:4][C:12]#[N:13]参加物
4
実験手順
To a heterogeneous slurry of 2-chloro-5-ethylaniline (1.6 g, 10 mmol) in 60 mL of water at 4° C. was added solid BrCN (0.848 g, 8 mmol) slowly. After 5 minutes the cooling bath was removed and the heterogeneous reaction mixture was stirred at room temperature for 24 hours to yield the product in water suspension. The precipitates were collected by filtration, washed with water (100 mL), and dried under vacuum to yield the pure title compound (1.45 g, 80% yield).
後処理
- customAfter 5 minutes the cooling bath was removed
- customto yield the product in water suspension
- filtrationThe precipitates were collected by filtration
- washwashed with water (100 mL)
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-63774565f3e0431f925976ea2cb9b52a
- 出典データセット
- uspto-grants-2000_11
- 特許番号
- US06153604
反応ノート
読み込み中…