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HRID 28148作成日:2026年10月25日

Allyl bromide → HCID 23339063、化合物

https://huagongshe.com/reaction/28148

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
溶媒BenzeneHCID 241—
生成物HCID 23339063HCID 23339063—

反応手順

To a stirring solution of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 3.8 parts of N-N-diethylethanamine in 200 parts of benzene are added portionwise 5 parts of 3-bromo-1-propene. After the addition is complete, the whole is heated for 21 hours at a temperature between 50°-60° C. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, dried over potassium carbonate and evaporated. The oily residue is converted into the hydrochloride salt in 1,1'-oxybisethane and 2-propanone, yielding 4 parts of N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochloride; mp. 225.5° 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-13f2a08e8f854d1fbf80096f4777ac60
出典メモuspto-grants-1980_09