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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412557Generated: October 27, 2026

Carbon tetrabromide → Benzyl 4-(bromomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/412557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 736490—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-(bromomethyl)piperidine-1-carboxylateHCID 277627489.9%

Reaction Steps

To a solution of 4-hydroxymethylpiperidine-1-carboxylic acid benzyl ester (1.11 g), carbon tetrabromide (1.77 g) in methylene chloride (11 ml) was added triphenylphosphine (1.4 g) with ice-cooling, and the mixture was stirred at room temperature for 5 hours. After completion of the reaction, the solvent was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:acetone=10:1) and dried under reduced pressure to give the title compound (1.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562828B1
Source datasetuspto-grants-2003_05
ORD IDord-712740cb1d5a420db17ae984c0c3ade2
Source noteuspto-grants-2003_05