HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220042Generated: October 30, 2026
Potassium Carbonate → Methyl 5-(4-(1,1-difluoroethyl)phenyl)nicotinate
https://huagongshe.com/reaction/220042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 1-Bromo-4-(1,1-difluoroethyl)benzene | HCID 45158847 | — |
| Reactant | [5-(Methoxycarbonyl)pyridin-3-yl]boronic acid hydrochloride | HCID 66890177 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 5-(4-(1,1-difluoroethyl)phenyl)nicotinate | HCID 58116582 | — |
Reaction Steps
A solution of 2.98 g (13.3 mmol) of the compound from Example 48A in toluene (25.0 ml) was admixed under argon at RT with 3.62 g (16.7 mmol) of the compound from Example 33A in ethanol (8.4 ml) and 2.03 g (14.7 mmol) of potassium carbonate. After stirring for 10 min, 1.54 g (1.34 mmol) of tetrakis(triphenylphosphine)palladium and then 2.33 g (40.0 mmol) of potassium fluoride in water (5.8 ml) were added. The mixture was stirred under reflux for 8 h, and the reaction solution was cooled and diluted with ethyl acetate. The reaction solution was washed in water, and the organic phase was dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by means of column chromatography (silica gel, dichloromethane/methanol 100:1→80:1). Yield: 2.62 g (69% of theory, 4:1 mixture of methyl and ethyl ester)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202862B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-6a36d0dad148411fad4263377068b6fe |
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| Source note | uspto-grants-2012_06 |
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