HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577176Generated: October 28, 2026
Ethyl 3-bromo-5-fluoropyridine-4-carboxylate → HCID 59589366, compound
https://huagongshe.com/reaction/577176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-bromo-5-fluoropyridine-4-carboxylate | HCID 46311470 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59589366 | HCID 59589366 | 51% |
Reaction Steps
To a solution of ethyl 3-bromo-5-fluoropyridine-4-carboxylate (4.8 g, 20 mmol) in anhydrous 1,4-dioxane (30 mL) at room temperature was added (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium (II) (325 mg, 0.43 mmol), followed by a diethylzinc solution (22 mL, 20 mmol, 1.1 M solution in toluene). The mixture was stirred at 70° C. for 45 minutes. After cooling to room temperature, the reaction was quenched with MeOH. Ethyl acetate (100 mL) was added. The mixture was extracted with 0.1 N HCl (200 mL). The organic layer was recovered. The pH of the aqueous phase was brought to 6 with 2 N NaOH. The mixture was extracted with EtOAc (1×100 mL). The combined organic extracts were dried over MgSO4, filtered, evaporated, and dried in vacuo. The crude product was purified by flash chromatography (0-20% ethyl acetate/hexane), affording ethyl 3-ethyl-5-fluoropyridine-4-carboxylate (2.0 g, 51% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040538B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-0c3346e332434df98ab0a31bc97fe2e8 |
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| Source note | uspto-grants-2015_05 |
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