4-Chlorobenzoyl chloride → 4-Chloro-N-(4-methyl-2-oxopentyl)benzamide
反応式
Cl.[C:2]([CH2:8][NH2:9])(=[O:7])[CH2:3][CH:4]([CH3:6])[CH3:5].C(=O)(O)[O-].[Na+].[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([C:20](Cl)=[O:21])=[CH:18][CH:17]=1>>[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([C:20]([NH:9][CH2:8][C:2](=[O:7])[CH2:3][CH:4]([CH3:6])[CH3:5])=[O:21])=[CH:18][CH:17]=1参加物
4
実験手順
3.8 g of isovalerylmethylamine hydrochloride, 5.04 g of sodium bicarbonate and 4.9 g of 4-chlorobenzoyl chloride are treated in the same manner as described in Preparation 1-(4). 6.2 g of N-(4-chlorobenzoyl)isovalerylmethylamine are thereby obtained. Yield: 98.0.
後処理
- customas described in Preparation 1-(4)
出典と根拠
- ORDレコード
- ord-7ca0d74dc2174541b0f38c4a8420904b
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04535089
反応ノート
読み込み中…