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4-Toluenesulfonyl chloride → (R)-3-tosyloxymethyl-1-methylpiperidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 反応物 | (R)-(1-methylpiperidin-3-yl)methanol | HCID 920113 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (R)-3-tosyloxymethyl-1-methylpiperidine | HCID 15895222 | 42.3% |
反応手順
A solution of (R)-3-hydroxymethyl-1 -methylpiperidine (2.6 g, 20 mmol) in dichloromethane (70 mL) was cooled to 5° C. and tosyl chloride (3.8 g, 20 mmol) was added in portions during 15 minutes. After the addition was complete, the reaction was allowed to warm to room temperature and was stirred for 20 hours. The reaction mixture was then concentrated and the residue partitioned between 10% potassium hydroxide (50 mL) and ether (100 mL). The ether layer was removed and the aqueous phase extracted once again with ether (50 mL). The combined ether layers were dried over magnesium sulfate and concentrated to afford (R)-3-tosyloxymethyl-1 -methylpiperidine as a white solid (2.4 g, 42%), m.p. 74.5-81.0° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06262078B1 |
| 出典データセット | uspto-grants-2001_07 |
| ORD ID | ord-109302689e704cf1a2f324624ab9d0fb |
| 出典メモ | uspto-grants-2001_07 |