Ethylene Oxide → 2-[Benzyl(2-hydroxyethyl)amino]benzamide
反応式
[CH2:1]([NH:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:18]1[O:20][CH2:19]1>C(O)(=O)C>[CH2:1]([N:8]([CH2:18][CH2:19][OH:20])[C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
o-Benzylaminobenzamide (62 g) was added to a cold solution of 85 ml ethylene oxide in 500 ml acetic acid, the mixture stirred 22 hours at room temperature and concentrated on the rotovap to remove 250 ml acetic acid. The remainder was made alkaline with 10% NaOH and the solid filtered washed with water and recrystallized from 300 ml ethyl acetate to give 48.5 g. product, m. 133-7.
後処理
- concentrationconcentrated on the rotovap
- customto remove 250 ml acetic acid
- filtrationthe solid filtered
- washwashed with water
- customrecrystallized from 300 ml ethyl acetate
- customto give 48.5 g
出典と根拠
- ORDレコード
- ord-eea9a560cead4d6395ea84d6a9a4e48c
- 出典データセット
- uspto-grants-1980_05
- 特許番号
- US04205173
反応ノート
読み込み中…