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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403565Generated: October 30, 2026

3-Bromobenzyl bromide → Benzenemethanamine, 3-bromo-N-ethyl-

https://huagongshe.com/reaction/2403565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantHCID 86635283HCID 86635283—
ProductBenzenemethanamine, 3-bromo-N-ethyl-HCID 45758971.2%

Reaction Steps

To 80% ethylamine/MeOH (1.1 g) was added 1-bromo-3-(bromomethyl)benzene (1 g) in five divided portions at room temperature, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the obtained residue was subjected to liquid separation with chloroform and a saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated, and then the aqueous layer was extracted with CHCl3 again. These organic layers were combined, dried over Na2SO4, and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH silica, 3% MeOH/CHCl3) to obtain N-(3-bromobenzyl)ethanamine (610 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-eeb8e6bc287847d8bc7ed3e85461c726
Source noteuspto-grants-2014_08