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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251607Generated: November 1, 2026

Water → 1,2-Bis-benzyloxy-3-bromo-5-trifluoromethyl-benzene

https://huagongshe.com/reaction/2251607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Benzenediol, 3-bromo-5-(trifluoromethyl)-HCID 59643037—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product1,2-Bis-benzyloxy-3-bromo-5-trifluoromethyl-benzeneHCID 59643024—

Reaction Steps

To a solution of 3-bromo-5-trifluoromethyl-benzene-1,2-diol (510 mg, 1.98 mmol) in 10 mL acetone, K2CO3 (2.74 g, 19.84 mmol, 10 eq.) and benzyl bromide (1.02 g, 5.95 mmol, 3 eq.) were added and the solution was refluxed for 4 h. After cooling to r.t., H2O and EtOAc were added to the mixture and the phases were separated The organic fraction was washed with saturated NaCl solution, dried over MgSO4 and evaporated in vacuo. The crude product was purified using flash chromatography (silica gel, hexane/EtOAc 10:1) to yield the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319101B2
Source datasetuspto-grants-2008_01
ORD IDord-358d3336000e4671bd5237234139eec0
Source noteuspto-grants-2008_01