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HRID 236755作成日:2026年10月25日

Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine

https://huagongshe.com/reaction/236755

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TriethylamineHCID 8471—
反応物N-(4-chlorophenyl)piperidin-4-amineHCID 7183033—
溶媒BenzeneHCID 241—
生成物N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamineHCID 23339007—

反応手順

To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20h. 30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04157393
出典データセットuspto-grants-1979_06
ORD IDord-98e53cc324e84b83a60aa09d13d4d66e
出典メモuspto-grants-1979_06