HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503685Generated: October 30, 2026
Potassium Carbonate → 2-(Trifluoromethoxy)-4-vinylbenzoic acid
https://huagongshe.com/reaction/1503685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-(trifluoromethoxy)benzoic acid | HCID 16665572 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Trifluoromethoxy)-4-vinylbenzoic acid | HCID 89306373 | 47% |
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]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212164B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e36c412f68c441aa851c1fc40f14c0c9 |
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| Source note | uspto-grants-2015_12 |
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