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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842037Generated: October 30, 2026

Benzyl Bromide → 2-Benzyloxy-5-(trifluoromethoxy)bromobenzene

https://huagongshe.com/reaction/842037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-(trifluoromethoxy)phenolHCID 21584090—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Benzyloxy-5-(trifluoromethoxy)bromobenzeneHCID 1129096696.5%

Reaction Steps

2-Bromo-4-(trifluoromethoxy)phenol (5 g, 20 mmol) was dissolved in N,N-dimethylformamide (60 ml), and potassium carbonate (5.4 g, 40 mmol) was added, followed by benzyl bromide (3.5 ml, 30 mmol), and the reaction was stirred at ambient temperature for 15 hours. The reaction was diluted with water (150 ml) and extracted into ethyl acetate (3×60 ml). The combined organic fractions were washed with water (100 ml), brine (100 ml), dried (MgSO4) and evaporated in vacuo. Purification on silica, eluting with 2% and 5% ethyl acetate in hexane gave the title compound as a clear oil (6.7 g, 96%). 1H NMR (250 MHz, CDCl3) δ 5.47 (2H, s), 7.23 (1H, d, J 9 Hz), 7.43 (1H, dd J 8.2, 2.9 Hz), and 7.75 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372754B1
Source datasetuspto-grants-2002_04
ORD IDord-6422b943c8c34ebd82a55f33d506eab7
Source noteuspto-grants-2002_04