HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963219Generated: October 30, 2026
Hydrochloric Acid → Methyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochloride
https://huagongshe.com/reaction/1963219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-chloropyridine-4-carboxylate | HCID 2736842 | — |
| Reactant | 2-Fluoro-4-(trifluoromethyl)benzeneboronic acid | HCID 16414145 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Methyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochloride | HCID 66732338 | 99% |
Reaction Steps
Methyl 2-chloroisonicotinate (2.8 g, 16.32 mmol), 2-fluoro-4-(trifluoromethyl)phenylboronic acid (5.09 g, 24.48 mmol), potassium carbonate (1.692 g, 12.24 mmol) and PdCl2 (dppf) (0.354 g, 0.49 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 dark-orange solid. The solid was dissolved in MTBE and stirred for 15 minutes, then filtered. The orange MTBE layer was treated with hydrogen chloride (4 M in dioxane, 4.08 mL, 16.32 mmol) and stirred for 1 h at room temperature. The precipitate was collected by filtration. Methyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochloride (5.4 g, 99%) was isolated as a slightly orange solid. MS m/z 300 (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-766f86eed66f479ea83c4d4c0eb803be |
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| Source note | uspto-grants-2013_04 |
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