Thionyl Chloride → 29030-58-8
反応式
[CH:1]1([C:7]2[CH:12]=[CH:11][C:10]([CH2:13][C:14]([NH2:16])=O)=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.S(Cl)(Cl)=O>>[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]([CH2:13][C:14]#[N:16])=[CH:11][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1参加物
3
実験手順
17.3 g of para-cyclohexyl-phenylacetamide and 35 ml of thionyl chloride are stirred at 70°C for 3 hours. The excess thionyl chloride is evaporated, the residue dissolved in ethyl acetate, and the solution washed with sodium bicarbonate solution and water. The solvent is evaporated and the residue distilled in a high vacuum. There is obtained paracyclohexylphenylacetonitrile boiling at 131°-132°C under a pressure of 0.35 mm of Hg and melting at 48°-49°C.
後処理
- customThe excess thionyl chloride is evaporated
- dissolutionthe residue dissolved in ethyl acetate
- washthe solution washed with sodium bicarbonate solution and water
- customThe solvent is evaporated
- distillationthe residue distilled in a high vacuum
出典と根拠
- ORDレコード
- ord-ba90b6daa13f4762869b6b85a7d2c976
- 出典データセット
- uspto-grants-1976_07
- 特許番号
- US03968142
反応ノート
読み込み中…