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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502965Generated: October 30, 2026

Potassium Carbonate → 2-(Trifluoromethoxy)-4-vinylbenzoic acid

https://huagongshe.com/reaction/1502965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-(trifluoromethoxy)benzoic acidHCID 16665572—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-(Trifluoromethoxy)-4-vinylbenzoic acidHCID 8930637347%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 4-bromo-2-(trifluoromethoxy)benzoic acid (1 g, 3.67 mmol) in DMSO (20 mL) was added potassium vinyltrifluoroborate (1.47 g, 11.02 mmol) and potassium carbonate (1.52 g, 11.02 mmol). The reaction mixture was degassed with argon for 30 min Bistriphenylphosphine(diphenylphosphinoferrocene)palladium dichloride (0.13 g, 0.18 mmol) was added and the reaction mixture was heated to 80° C. for 1 h. The reaction mixture was diluted with water (100 mL), extracted with ethyl acetate (2×50 mL), washed with brine, and dried over Na2SO4. Concentration under reduced pressure furnished the crude compound which was purified by flash column chromatography to afford the product as pale yellow gummy material (0.4 g, 47%): 1H NMR (400 MHz, CDCl3) δ 8.05 (d, J=8.1 Hz, 1H), 7.44 (d, J=1.8 Hz, 1H), 7.35 (s, 1H), 6.78 (dd, J=17.4.1, 11.1 Hz, 1H), 5.92 (d, J=17.4 Hz, 1H), 5.51 (d, J=10.8 Hz, 1H); ESIMS m/z 232.97 ([M+H]E).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211281B2
Source datasetuspto-grants-2015_12
ORD IDord-33ca3d74cbba43e99cdd2e225912df57
Source noteuspto-grants-2015_12