反応式
[C:1]1([CH:7](O)[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(C(C)C)C(C)C)C.CS([Cl:24])(=O)=O>ClCCl.C(=O)(O)[O-].[Na+]>[Cl:24][CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH2:8][CH3:9]参加物
6
実験手順
Under ice cooling, to a solution of 1-phenyl-1-propanol (1.0 g, 7.34 mmol) and N-ethyldiisopropylamine (1.42 g, 11.01 mmol) in dichloromethane (10 ml) was added methanesulfonyl chloride (690 μl, 8.81 mmol), and the mixture was stirred at room temperature for 5 hours. The reaction mixture was diluted with saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent:ethyl acetate/hexane:5/1) to give 1-chloro-1-phenylpropane (610 mg, 54%) as pale yellow liquid.
後処理
- extractionextracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried over magnesium sulfate, and solvent
- distillationwas distilled off under reduced pressure
- customThe residue was purified by silica gel chromatography (eluent:ethyl acetate/hexane:5/1)
出典と根拠
- ORDレコード
- ord-220ff6ae2e7c40578a6107e441c96209
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058280B2
関連ノート
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