Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403785Generated: October 31, 2026

Hydrogen Bromide → 3-(Bromomethyl)-1-ethylpiperidine

https://huagongshe.com/reaction/2403785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(1-Ethylpiperidin-3-yl)methanolHCID 20439432—
SolventDichloromethaneHCID 6344—
Product3-(Bromomethyl)-1-ethylpiperidineHCID 21510488—

Reaction Steps

48% Aqueous hydrogen bromide (16 ml) was added to N-ethyl-3-piperidinemethanol (1.53 g) and the stirring mixture refluxed for 6 hours. After cooling, the solvent was stripped, the residue treated with water and made basic by addition of 1M aq. potassium carbonate. The mixture was shaken with dichloromethane, filtered to remove unwanted solid, and the filtrate separated. The aqueous layer was further extracted with dichloromethane and the combined extracts washed with dilute brine, dried by passing through a phase separation cartridge and stripped to give the title compound as a pale oil (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-cd20639462064565b1a77adab394ac84
Source noteuspto-grants-2014_08