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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616041Generated: October 30, 2026

Allyl bromide → 3-(3,4-Dimethoxyphenyl)-1-(prop-2-en-1-yl)piperidine

https://huagongshe.com/reaction/616041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant3-(3,4-Dimethoxyphenyl)piperidineHCID 12937921—
CatalystSilver(II) oxideHCID 92152—
SolventAcetoneHCID 180—
Product3-(3,4-Dimethoxyphenyl)-1-(prop-2-en-1-yl)piperidineHCID 20370848—

Reaction Conditions

Temperature20 °C

Reaction Steps

2.8 g of silver oxide were added to a solution of 5.6 g of 3-(3',4'-dimethoxyphenyl)-piperidine in 28 ml of acetone and then 2.3 ml of allyl bromide were added dropwise thereto with slow cooling. The mixture was stirred at 20° C for 30 minutes and was then filtered. The filtrate was evaporated to dryness and the residue was chromatographed over silica gel. Elution with a 6-3-1 cyclohexane-chloroform-triethylamine mixture yielded 5.55 g of N-allyl-3-(3',4'-dimethoxyphenyl)-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072685
Source datasetuspto-grants-1978_02
ORD IDord-9520700508b8411ca156d8943583fdae
Source noteuspto-grants-1978_02