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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420822Generated: November 1, 2026

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

https://huagongshe.com/reaction/1420822

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 (Description 11; 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 h. 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) δ5.47 (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 numberUS06071927
Source datasetuspto-grants-2000_06
ORD IDord-a278fc56af0144739c7ecbc6fe23eab6
Source noteuspto-grants-2000_06