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HRID 222574作成日:2026年10月26日

Triethylamine → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/222574

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Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 276583888.1%

反応条件

温度23 °C

反応手順

Methanesulfonyl chloride (29.26 g, 19.77 mL, 255.47 mmol) is added slowly (10 min) under nitrogen atmosphere to a solution of tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate (50.00 g, 232.24 mmol) and triethylamine (35.25 g, 48.56 mL, 348.36 mmol) in anhydrous dichloromethane (700 mL) at 9° C. (internal temperature). The mixture is stirred at 23° C. for 16 h. The reaction mixture is successively washed with 1 M aq hydrochloric acid, water, and brine. The organic layer is dried over anhydrous sodium sulfate, filtered, and the solvent is removed to obtain 60 g of the title compound as a white solid. MS (m/z) 316 (M+23).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207344B2
出典データセットuspto-grants-2012_06
ORD IDord-1f2372b8945d49749af2ffa4d7f146cf
出典メモuspto-grants-2012_06