HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963196Generated: October 26, 2026
Potassium Carbonate → Methyl 2-(3,4,5-trifluorophenyl)isonicotinate
https://huagongshe.com/reaction/1963196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3,4,5-Trifluorophenyl)boronic Acid (contains varying amounts of Anhydride) | HCID 2734671 | — |
| Reactant | 2-Bromo-isonicotinic acid methyl ester | HCID 3847768 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3,4,5-trifluorophenyl)isonicotinate | HCID 66732308 | 52.9% |
Reaction Steps
Methyl 2-bromoisonicotinate (4 g, 18.52 mmol), 3,4,5-trifluorophenylboronic acid (4.89 g, 27.77 mmol), potassium carbonate (3.84 g, 27.77 mmol) and PdCl2 (dppf) (0.402 g, 0.56 mmol) were mixed in methanol (30 mL) in two separate 20 mL microwave vials. The vials were capped and heated at 100° C. for 10 min in a single node microwave reactor. Water and DCM were added and the phases were separated. The water phase (pH 9) was extracted with DCM and the combined organic phase washed with brine, passed through a phase separator and evaporated to yield a brown solid. The residue was dissolved in DCM and purified by SCX-2 cation exchange chromatography. Methyl 2-(3,4,5-trifluorophenyl)isonicotinate (2.62 g, 52%) was isolated as a slightly yellow solid. MS m/z 268 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415378B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-5c8f2e49c53b41fd866ec5ae6c644456 |
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| Source note | uspto-grants-2013_04 |
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