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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397678Generated: October 27, 2026

Carbon tetrabromide → Benzyl 3-(bromomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/397678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantBenzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—
ProductBenzyl 3-(bromomethyl)piperidine-1-carboxylateHCID 23000675—

Reaction Steps

The title compound was prepared by the method of Preparation 9 from benzyl 3-(hydroxymethyl)-1-piperidinecarboxylate [Preparation 59] and carbon tetrabromide. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 0:100 changing to 80:20, by volume ethyl acetate:hexane, in 10% increments, to afford benzyl 3-(bromomethyl)-1-piperidinecarboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-164ee47031954a3db82e5c0dac7edea4
Source noteuspto-grants-2003_08