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HRID 522628作成日:2026年10月26日

Triethylamine → (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/522628

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 (2S)-2-(hydroxymethyl)morpholine-4-carboxylateHCID 1512577—
溶媒DichloromethaneHCID 6344—
生成物(S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylateHCID 8667356798.1%

反応条件

温度0 °C

反応手順

To a solution of (S)-tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (3.0 g, 13.8 mmol) and triethylamine (4.2 g, 41.4 mmol) in dichloromethane (80 mL) at 0° C. was dropwise added mesyl chloride (1.9 g, 16.5 mmol). The reaction mixture was stirred at 0° C. for 2 hour, and then diluted with dichloromethane (100 mL). The organic layers were washed with water (100 mL) and brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate as a purple oil (4.0 g, 98%), which was directly used in the next step without further purification. MS (ES+) C11H21NO6S requires: 295, found: 240 [M+H-56]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334263B2
出典データセットuspto-grants-2016_05
ORD IDord-d8089c48fc6c46bfad3a755251fe9aa4
出典メモuspto-grants-2016_05