Dimethyl Sulfide → 2-(4-Iodophenyl)-2-methyloxirane
反応式
CSC.S([O:9][CH3:10])(OC)(=O)=O.[CH3:11][C:12]([C:14]1[CH:19]=[CH:18][C:17]([I:20])=[CH:16][CH:15]=1)=O.C[O-].[Na+]>C(#N)C>[I:20][C:17]1[CH:18]=[CH:19][C:14]([C:12]2([CH3:11])[CH2:10][O:9]2)=[CH:15][CH:16]=1参加物
反応条件
- 温度
- 25 °C
実験手順
To a solution of 30 g of dimethyl sulfide in 30 ml of acetonitrile was added dropwise over a period of 30 minutes 30 g of dimethyl sulfate, while maintaining the temperature at 40° to 50° C., and the mixture was stirred for one hour at the same temperature. The reaction mixture was cooled to 25° C. and mixed with 30 g of 4-iodoacetophenone and 90 ml of acetonitrile. While stirring, 13.2 g of sodium methoxide was added to the mixture and stirring was continued for a further 30 minutes at room temperature to complete the reaction. Thereafter, the dimethyl sulfide and acetonitrile were removed by distillation, and to the residue were added 120 ml of cyclohexane and 120 ml of water, after which the mixture was thoroughly shaken. The organic layer was separated, dried over anhydrous magnesium sulfate, and freed from the solvent by distillation under reduced pressure to obtain 31.5 g (99% yield) of oily 2-(4-iodophenyl)-2-methyloxirane having a melting point of 44°-45° C.
後処理
- temperaturewhile maintaining the temperature at 40° to 50° C.
- stirringWhile stirring
- stirringstirring
- waitwas continued for a further 30 minutes at room temperature
- customthe reaction
- customThereafter, the dimethyl sulfide and acetonitrile were removed by distillation
- additionto the residue were added 120 ml of cyclohexane and 120 ml of water
- stirringafter which the mixture was thoroughly shaken
- customThe organic layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- distillationfreed from the solvent by distillation under reduced pressure
出典と根拠
- ORDレコード
- ord-975c4c8ded5a4cf8b32ea5624bac350c
- 出典データセット
- uspto-grants-1980_10
- 特許番号
- US04230719
反応ノート
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