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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704418Generated: October 26, 2026

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

https://huagongshe.com/reaction/1704418

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126689
Source datasetuspto-grants-1978_11
ORD IDord-1f6bf37f4aa04adb933352b15139e5b7
Source noteuspto-grants-1978_11