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HRID 1384974作成日:2026年10月27日

4-Toluenesulfonyl chloride → (R)-3-tosyloxymethyl-1-methylpiperidine

https://huagongshe.com/reaction/1384974

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物(R)-(1-methylpiperidin-3-yl)methanolHCID 920113—
溶媒DichloromethaneHCID 6344—
生成物(R)-3-tosyloxymethyl-1-methylpiperidineHCID 1589522242.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06262078B1
出典データセットuspto-grants-2001_07
ORD IDord-109302689e704cf1a2f324624ab9d0fb
出典メモuspto-grants-2001_07