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Triethylamine → (2-Chloropyridin-4-yl)methyl methanesulfonate
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 | (2-Chloropyridin-4-yl)methanol | HCID 7062237 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2-Chloropyridin-4-yl)methyl methanesulfonate | HCID 53436764 | 68.4% |
反応手順
To a stirred solution of (2-chloropyridin-4-yl)methanol (0.500 g, 3.496 mmol) in dichloromethane (15 mL), triethylamine (0.424 g, 4.195 mmol) and methanesulfonylchloride (0.440 g, 3.846 mmol) were added at 0° C. and stirred at room temperature for 2-3 h. The reaction was quenched with water and extracted with dichloromethane. The organic layer was concentrated in vacuo to give (2-chloropyridin-4-yl)methyl methanesulfonate (0.530 g, 68%); MS: 221.9 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09000175B2 |
| 出典データセット | uspto-grants-2015_04 |
| ORD ID | ord-dbe6dcafa19e4fc0b55dd62ddede6b56 |
| 出典メモ | uspto-grants-2015_04 |