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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964937Generated: November 2, 2026

Benzyl Bromide → 1-Benzyloxy-2-chloro-4-fluorobenzene

https://huagongshe.com/reaction/1964937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-4-fluorophenolHCID 74814—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyloxy-2-chloro-4-fluorobenzeneHCID 5808673164.2%

Reaction Steps

To a solution of 2-chloro-4-fluorophenol (617, 7 g, 0.05 mol) in tetrahydrofuran (100 mL) was added sodium hydride (1.8 g, 95% dry powder, 0.071 mol) at room temperature over 15 minutes under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 30 minutes. Benzyl bromide (10 g, 0.060 mol) was added slowly to the reaction mixture, then stirred at room temperature overnight. The reaction mixture was poured into ice water, extracted with ethyl acetate, washed with hydrochloric acid (10%), water, brine, and dried over magnesium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with ethyl acetate in hexane to provide compound as a white solid (618, 7.6 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415469B2
Source datasetuspto-grants-2013_04
ORD IDord-4d76fa63834c42d9af62176e8c40b181
Source noteuspto-grants-2013_04