反応式
[OH:1][CH:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>C(Cl)Cl>[CH3:15][S:16]([N:5]1[CH2:6][CH2:7][CH:2]([O:1][S:16]([CH3:15])(=[O:18])=[O:17])[CH2:3][CH2:4]1)(=[O:18])=[O:17]参加物
5
実験手順
To a solution of 4-hydroxypiperidine (5.10 g, 50 mmoles) and triethylamine (20.9 ml, 150 mmoles) in methylene chloride (150 ml) was added methanesulfonyl chloride (8.54 ml, 110 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was solidified with ethyl acetate-n-hexane to obtain 11.45 g of the desired product (88.3%, pale yellow solid).
後処理
- temperaturecooling
- stirringthe mixture was stirred at room temperature for 1 hour
- washThe reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline
- dry with materialdried over anhydrous magnesium sulfate
- distillationAfter the solvent was distilled off
出典と根拠
- ORDレコード
- ord-b3730f138bfa468185545870673f245b
- 出典データセット
- uspto-grants-1996_12
- 特許番号
- US05587383
関連ノート
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