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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192701Generated: October 26, 2026

Methanol → 1-[4-(4-Bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanone

https://huagongshe.com/reaction/2192701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2',4'-DihydroxyacetophenoneHCID 6990—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-fluorobenzyl bromideHCID 2733660—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanoneHCID 6698823875.4%

Reaction Steps

1-(2,4-dihydroxyphenyl)ethanone (25.3 g, 0.17 mol) and 4-bromo-1-bromomethyl-2-fluorobenzene (44.6 g, 0.17 mol) were dissolved in DMF (150 mL). Potassium carbonate (11.8 g, 0.09 mol) was added to the solution under ice-cooled conditions, and the mixture was stirred under ice-cooled conditions and further stirred at room temperature for 12 hours. Again, potassium carbonate (11.8 g, 0.09 mol) was added to the mixture under ice-cooled conditions, and the mixture was stirred under ice-cooled conditions for 30 minutes and further stirred at room temperature for 12 hours. Methanol (100 mL) was added to this reaction solution, and the mixture was stirred at 80° C. for 1 hour. Thereafter, water (150 mL) was added to the mixture, and precipitated crystals were filtered and washed with methanol. The crystals were vacuum-dried at 60° C. for 2 hours, yielding 1-[4-(4-bromo-2-fluorobenzyloxy)-2-hydroxyphenyl]ethanone (43.5 g, yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329739B2
Source datasetuspto-grants-2012_12
ORD IDord-007942aad0dc467980dae15584f6932f
Source noteuspto-grants-2012_12