Ammonia → Benzhydrylthioacetamide
反応式
[NH3:1].[CH:2]([CH2:15][C:16](Cl)=[S:17])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>O.C(Cl)Cl>[CH:2]([CH2:15][C:16]([NH2:1])=[S:17])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1参加物
5
実験手順
35 ml of ammonia in 40 ml of water are introduced into a three-necked flask provided with a condenser and a dropping funnel and the benzhydrylthioacetyl chloride dissolved in about 100 ml of methylene chloride is added drop by drop. Once the addition is complete, the organic phase is washed with a dilute solution of soda and dried over Na2SO4, the solvent is evaporated and the residue is taken up in diisopropyl ether; in this way, the benzhydrylthioacetamide is crystallised. 16.8 g of product (yield=86%) are obtained.
後処理
- customprovided with a condenser and a dropping funnel
- additionis added drop by drop
- additionOnce the addition
- washthe organic phase is washed with a dilute solution of soda
- dry with materialdried over Na2SO4
- customthe solvent is evaporated
- customin this way, the benzhydrylthioacetamide is crystallised
出典と根拠
- ORDレコード
- ord-6a28b1ce8efc4f119f9f8b2abce79ac7
- 出典データセット
- uspto-grants-1979_12
- 特許番号
- US04177290
反応ノート
読み込み中…