HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810980Generated: November 2, 2026
Potassium Carbonate → HCID 57516327, compound
https://huagongshe.com/reaction/1810980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | Methyl 2,6-dichloro-5-fluoronicotinate | HCID 2775354 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57516327 | HCID 57516327 | 45.8% |
Reaction Steps
A mixture of 2,6-dichloro-5-fluoro-nicotinic acid methyl ester (1.00 g 4.46 mmol), trimethylboroxin (0.620 mL, 4.40 mmol), tetrakis(triphenylphosphine)palladium (0.500 g, 0.433 mmol) and potassium carbonate (1.50 g, 12.0 mmol) is heated at 110° C. overnight. The mixture is cooled to room temperature, diluted with water, and extracted with EtOAc. The combined organic phase is washed with water followed by brine, then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by flash silica gel chromatography using a gradient of 0-30% EtOAc/heptane to provide 0.410 g (45.1%) of 2-chloro-5-fluoro-6-methyl-nicotinic acid methyl ester as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362249B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-f1eb6dc9169846bdbd3110794dea672e |
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| Source note | uspto-grants-2013_01 |
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