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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706740Generated: October 26, 2026

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

https://huagongshe.com/reaction/1706740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
ReactantN-(4-chlorophenyl)piperidin-4-amineHCID 7183033—
SolventBenzeneHCID 241—
ProductN-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamineHCID 23339007—

Reaction Steps

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 20 h. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208418
Source datasetuspto-grants-1980_06
ORD IDord-d61adeda6bea47adb421d39c325ec38a
Source noteuspto-grants-1980_06