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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403800Generated: November 3, 2026

Carbon tetrabromide → Benzyl 2-(2-bromoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2403800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 2-(2-hydroxyethyl)piperidine-1-carboxylateHCID 45358666—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-(2-bromoethyl)piperidine-1-carboxylateHCID 5830621074.1%

Reaction Steps

To a solution of phenylmethyl 2-(2-hydroxyethyl)-1-piperidinecarboxylate (1.76 g, 6.70 mmol) in anhydrous dichloromethane (29 mL) was added carbon tetrabromide (4.44 g, 13.39 mmol). The resulting solution was cooled in ice/water. A solution of triphenylphosphine (1.76 g, 6.70 mmol) in 10 ml dry DCM was added dropwise over 30 mins. After complete addition the reaction was allowed to warm slowly to ambient temperature and stirring continued overnight. The reaction solution was reduced in volume to <10 ml (opaque) and this was loaded onto a 100 g silica cartridge and purified by chromatography on a Flashmaster 2 using a gradient of 0-25% ethyl acetate in cyclohexane over 40 minutes. Product fractions were combined and evaporated in vacuo to give the title compound as a colourless oil (1.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-a2f9634db9274a9e8174aa882ac46731
Source noteuspto-grants-2014_08