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HRID 382779作成日:2026年10月26日

4-Benzylpiperidine → 4[-2-(4-Benzyl-piperidine-1-yl)-ethanesulfonyl]-phenol

https://huagongshe.com/reaction/382779

反応式

関与物質

役割名称HCID仕込み量
反応物4-BenzylpiperidineHCID 31738—
反応物4-(2-Chloro-ethanesulfonyl)-phenolHCID 9813249—
溶媒DichloromethaneHCID 6344—
生成物4[-2-(4-Benzyl-piperidine-1-yl)-ethanesulfonyl]-phenolHCID 979894538.7%

反応手順

To a solution of 40.0 g 4-(2-chloro-ethanesulfonyl)-phenol (181 mmol) in 600 ml CH2Cl2 were added 69.9 g 4-benzylpiperidine (399 mmol). After stirring for 16 h at r. t. the reaction mixture was concentrated to 100 ml and directly purified by chromatography over silica gel (CH2Cl2/MeOH/NH3 19/1/0.1). Recrystallization from ethyl acetatelhexane (2:1) yielded 25 g product (70 mmol, 38%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310213B1
出典データセットuspto-grants-2001_10
ORD IDord-840af965b37549a1b786c559c48d75aa
出典メモuspto-grants-2001_10