関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | tert-Butyl (2S)-2-(hydroxymethyl)morpholine-4-carboxylate | HCID 1512577 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate | HCID 86673567 | 98.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09334263B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-d8089c48fc6c46bfad3a755251fe9aa4 |
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| 出典メモ | uspto-grants-2016_05 |
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