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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976063Generated: October 31, 2026

Benzyl Bromide → 2-Benzyloxy-3-bromo-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1976063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-Bromo-5-(trifluoromethyl)pyridin-2(1H)-oneHCID 13491775—
CatalystHCID 178418647HCID 178418647—
SolventHexaneHCID 8058—
Product2-Benzyloxy-3-bromo-5-trifluoromethylpyridineHCID 2200019891.3%

Reaction Steps

3-Bromo-5-trifluoromethyl-2(1H)-pyridone (6.09 g, 25.2 mmol) and silver carbonate (7.18 g, 26.0 mmol) were suspended in hexane (200 mL) and treated with benzyl bromide (6 mL, 50.3 mmol). The mixture was stirred for 18 hrs, then filtered. The filtrate was concentrated and the residue purified by silica chromatography to give the product as a white solid (7.65 g, 23 mmol, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225320B1
Source datasetuspto-grants-2001_05
ORD IDord-33da332533ff41c3a8792822a9d935af
Source noteuspto-grants-2001_05