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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403433Generated: October 30, 2026

Carbon tetrabromide → tert-Butyl 2-(bromomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2403433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-(bromomethyl)piperidine-1-carboxylateHCID 2062435549.8%

Reaction Steps

To a solution of 4-hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (2.0 g) in anhydrous tetrahydrofuran (50 ml) was added carbon tetrabromide (6.2 g) and triphenylphosphine (4.88 g). the reaction mixture was stirred at room temperature for 3 days. The reaction mixture was filtered through celite. The filtrate was taken up in ethyl acetate, washed with water then brine, dried (MgSO4) and the solvent removed in vacuo give a crude product. This was purified using flash chromatography which yielded Bromomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.287 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802670B2
Source datasetuspto-grants-2014_08
ORD IDord-8d4dd3ddf3eb4e5cb2ef970d04b6c793
Source noteuspto-grants-2014_08