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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666470Generated: October 31, 2026

Water → 2-(3-Bromo-5-fluorophenoxy)-5-(trifluoromethyl)-pyridine

https://huagongshe.com/reaction/1666470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
Reactant3-Bromo-5-fluorophenolHCID 21904636—
SolventDimethylformamideHCID 6228—
Product2-(3-Bromo-5-fluorophenoxy)-5-(trifluoromethyl)-pyridineHCID 6687623498%

Reaction Steps

To a solution of 3-bromo-5-fluorophenol (2.54 g, 0.013 mol) in DMF (12 mL) under a N2 atmosphere was added potassium carbonate (3.59 g, 0.026 mol) and the reaction was stirred for 20 min at RT. 2-Chloro-5-trifluoromethylpyridine (2.4 g, 0.013 mol) was added and the reaction mixture was refluxed at 110° C. overnight. Water was added and the mixture was extracted with ethyl acetate three times. The organic layer was washed with brine, dried over Na2SO4 and evaporated to dryness. The residue was purified by silica gel column chromatography (10% ethyl acetate in hexane) to give the title compound (4.28 g, 96%). 1H NMR (500 MHz, CDCl3): δ 8.45 (s, 1H), 7.96 (dd, J=2 Hz, J=8.5 Hz, 1H), 7.16-7.15 (m, 2H), 7.08 (d, J=8.5 Hz, 1H), 6.89-6.85 (m, 1H); m/z (337.9, M+ H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-11bdcb2f5ad64ddab35d39656aae9754
Source noteuspto-grants-2011_10