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HRID 377421作成日:2026年10月25日

4-Toluenesulfonyl chloride → 1-(2-Chloroethyl)piperidine

https://huagongshe.com/reaction/377421

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1-(Piperidin-1-yl)ethanolHCID 3030541—
溶媒DichloromethaneHCID 6344—
生成物1-(2-Chloroethyl)piperidineHCID 74827—

反応手順

Into a 50 mL round bottom flask is placed 6.40 g (33.6 mmol) of p-toluenesulfonyl chloride and 25 mL of methylene chloride. The resulting solution is cooled with an ice bath as 4.00 g (31.0 mmol) of 1-piperidinoethanol in 6 mL of methylene chloride is added dropwise. After the addition is complete, the ice bath is removed and the resulting slurry is stirred for about 12 hours. The reaction mixture is concentrated on a rotary evaporator to yield a solid residue which may then be used as in Preparation 4 below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06025495
出典データセットuspto-grants-2000_02
ORD IDord-272121b4d9e74189a3251e5a42e2b264
出典メモuspto-grants-2000_02