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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17982Generated: October 26, 2026

Benzyl Bromide → 1-(Benzyloxy)-3-chloro-2-fluorobenzene

https://huagongshe.com/reaction/17982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Chloro-2-fluorophenolHCID 2773712—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-(Benzyloxy)-3-chloro-2-fluorobenzeneHCID 58592620—

Reaction Steps

A mixture of 3-chloro-2-fluorophenol (1.5 g, 10.2 mmol), benzyl bromide (1.71 g, 10.0 mmol) and sodium carbonate (1.10 g, 10.38 mmol) in 20 mL ethylene glycol dimethyl ether and 10 mL H2O was stirred at rt for 36 h. The reaction mixture was charged with 20 mL 1N KOH and 50 mL diethyl ether. The organic layer was separated, washed with brine, dried over sodium sulfate, and concentrated in vacuo to afford the title compound as a white solid which was used without further purification. 1H NMR (CDCl3, 400 MHz) δ 5.16 (s, 2Hs) 6.86-7.03 (m, 3Hs) 7.31-7.48 (m, 5Hs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741324B2
Source datasetuspto-grants-2010_06
ORD IDord-277708cca4ed4001a2f9f7525737ba56
Source noteuspto-grants-2010_06