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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403804Generated: October 30, 2026

Carbon tetrabromide → Benzyl 2-(3-bromopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2403804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 2-(3-hydroxypropyl)piperidine-1-carboxylateHCID 58306067—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-(3-bromopropyl)piperidine-1-carboxylateHCID 5830619081.1%

Reaction Steps

To a solution of phenylmethyl 2-(3-hydroxypropyl)-1-piperidinecarboxylate (2.14 g, 7.72 mmol) in anhydrous dichloromethane (34 ml) was added carbon tetrabromide (5.12 g, 15.43 mmol)). The resulting solution was cooled in ice/water. A solution of triphenylphosphine (4.05 g, 15.43 mmol) in 10 ml dry DCM was added dropwise over 30 mins., producing a deep amber/brown solution. After complete addition the reaction was allowed to warm slowly to ambient temperature and stirring continued overnight. The reaction mixture was filtered to remove the precipitate, washed with ether and the filtrate evaporated to approx 10 ml. This was then loaded onto a 100 g silica cartridge and purified by chromatography using a gradient of Flashmaster 0-25% ethylacetate in cylcohexane over 40 mins. on a Flashmaster collecting all the eluent. The product peak was identified by TLC and the fractions combined and evaporated in vacuo to give the title compound as a clear oil (2.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-47bb36af57db47dbb10ca09e542ccd87
Source noteuspto-grants-2014_08