HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8208Generated: October 25, 2026
Ethanol → Ethyl 5-fluoropyridine-2-carboxylate
https://huagongshe.com/reaction/8208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Bromo-5-fluoropyridine | HCID 2783171 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Product | Ethyl 5-fluoropyridine-2-carboxylate | HCID 10986675 | 58% |
Reaction Steps
A mixture of 2-bromo-5-fluoropyridine (5.00 g, 28.4 mmol), sodium acetate (9.33 g, 114 mmol), and 1-1′bis(diphenylphosphino)ferrocene]dichloropalladium(II):CH2Cl2 (0.464 g, 0.57 mmol) in ethanol (80 mL) in a Parr® high pressure stainless steel reactor vessel is placed under an atmosphere of 50 psi carbon monoxide and heated at 80-100° C. for 4 h. The vessel is cooled, volatiles removed in vacuo, and the residue partitioned between ethyl acetate and water. The ethyl acetate extract is washed with water and brine, dried over sodium sulfate, filtered, and evaporated to give a dark solid. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes) to yield the title compound 2.8 g (58%) as a white solid that is recrystallized from hexanes to give white crystals: mp 61-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087626B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-61b52ed67bce44c09e6ab3755fd6da79 |
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| Source note | uspto-grants-2006_08 |
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