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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603184Generated: November 1, 2026

Carbon tetrabromide → 3-(Bromomethyl)-1-ethylpiperidine

https://huagongshe.com/reaction/603184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
Reactant(1-Ethylpiperidin-3-yl)methanolHCID 20439432—
SolventTetrahydrofuranHCID 8028—
Product3-(Bromomethyl)-1-ethylpiperidineHCID 2151048869.5%

Reaction Steps

To mixture of (1-ethylpiperidin-3-yl)methanol (430 mg) and polymer bound triphenylphoshphine (2 g) in tetrahydrofuran (30 mL) was added carbon tetrabromide (1 g). The mixture was stirred for 8 hours before polymer bound triphenylphoshphine (1 g) and carbon tetrabromide (0.5 g) were added. The reaction was stirred overnight at room temperature. The mixture was filtered and evaporated and the residue was purified by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in dichloromethane to give the title compound as a yellow oil (430 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906645B2
Source datasetuspto-grants-2011_03
ORD IDord-c7b99397cc64466ea3dce4df42149760
Source noteuspto-grants-2011_03