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HRID 28151作成日:2026年10月25日

Triethylamine → N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride

https://huagongshe.com/reaction/28151

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-IodopropaneHCID 33643—
反応物N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
溶媒BenzeneHCID 241—
生成物N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochlorideHCID 23339041—

反応手順

To a stirred solution of 4 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide and 3 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 4 parts of 1-iodopropane and the whole is stirred and refluxed for 47 hours. Then the second portion of 4 parts of 1-iodopropane is added and stirring and refluxing is continued for another 20 h.20. The reaction mixture is cooled and filtered. The filtrate is washed with water, dried and evaporated in vacuo. From the oily free base, the hydrochloride salt is prepared in the conventional manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 3.5 parts of N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride; mp. 233.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225606
出典データセットuspto-grants-1980_09
ORD IDord-e2192b2ec0f648c4994e1497b6c9c192
出典メモuspto-grants-1980_09