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HRID 1608632作成日:2026年10月25日

Triethylamine → 1-(Methylsulfonyl)piperidin-4-yl methanesulfonate

https://huagongshe.com/reaction/1608632

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Piperidin-4-olHCID 79341—
溶媒DichloromethaneHCID 6344—
生成物1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 2227306588.3%

反応手順

To a solution of 4-hydroxypiperidine (5.10 g, 50 moles) and triethylamine (20.9 ml, 150 moles) 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05395839
出典データセットuspto-grants-1995_03
ORD IDord-22b0c675112e486e9006c7a9b55be52a
出典メモuspto-grants-1995_03