反応式
[CH3:1][CH:2]([NH:4][C:5]([C:7](=O)C=CC1C=CC=CC=1)=[O:6])[CH3:3].Cl[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([C:24]([O:26]O)=O)[CH:19]=1.S(C1C(C)=CC(O)=C(C(C)(C)C)C=1)C1C(C)=CC(O)=C(C(C)(C)C)C=1.C(Cl)CCl>C(Cl)(Cl)Cl>[CH3:1][CH:2]([NH:4][C:5]([CH:7]1[CH:24]([C:20]2[CH:19]=[CH:18][CH:23]=[CH:22][CH:21]=2)[O:26]1)=[O:6])[CH3:3]参加物
実験手順
A mixture of N-(1-methylethyl)cinnamoylcarboxamide (18 g.), m-chloroperbenzoic acid (23.6 g.), 4,4'-thiobis(6-tert-butyl-m-cresol) (0.3 g.) and ethylene dichloride (250 ml.) was heated under gentle reflux for 1 hour, then chilled in ice. A precipitate (m-chlorobenzoic acid) was separated by filtration and washed with ethylene dichloride. The filtrate and washings were combined, and evaporated under reduced pressure on a rotary evaporator to give an amber oil. The oil was dissolved in chloroform (300 ml.) and the chloroform solution was washed with 5% aqueous sodium bicarbonate solution twice, then with saline. The chloroform solution was dried over magnesium sulfate, then evaporated under reduced pressure in a rotary evaporator to give an oil. The oil solidified on standing. The solid mass was recrystallized from ether giving 8.4 g. of product, m.p. 114°-115°.
後処理
- temperaturewas heated
- temperatureunder gentle reflux for 1 hour
- temperaturechilled in ice
- customA precipitate (m-chlorobenzoic acid) was separated by filtration
- washwashed with ethylene dichloride
- customevaporated under reduced pressure on a rotary evaporator
- customto give an amber oil
- washthe chloroform solution was washed with 5% aqueous sodium bicarbonate solution twice
- dry with materialThe chloroform solution was dried over magnesium sulfate
- customevaporated under reduced pressure in a rotary evaporator
- customto give an oil
- customThe solid mass was recrystallized from ether giving 8.4 g
出典と根拠
- ORDレコード
- ord-fbb28a7930114db6a365e29ed5593b54
- 出典データセット
- uspto-grants-1983_08
- 特許番号
- US04401832
関連ノート
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