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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261090Generated: October 26, 2026

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

https://huagongshe.com/reaction/1261090

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 numberUS08470818B2
Source datasetuspto-grants-2013_06
ORD IDord-1122bf956dd04145a5cd14adb4f4bd20
Source noteuspto-grants-2013_06