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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650475Generated: October 26, 2026

Ethanol → Ethyl 5-chloro-3-fluoropicolinate

https://huagongshe.com/reaction/650475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant2,5-Dichloro-3-fluoropyridineHCID 10964877—
ReactantHCID 178418416HCID 178418416—
CatalystBis(triphenylphosphine)palladium chlorideHCID 84124—
CatalystHCID 178418476HCID 178418476—
ProductEthyl 5-chloro-3-fluoropicolinateHCID 22013569—

Reaction Conditions

Temperature90 °C

Reaction Steps

An autoclave is charged with 31.4 g of 2,5-dichloro-3-fluoropyridine, 400 ml of dry ethanol, 27.8 ml of triethylamine and 3.5 g of palladium bis(triphenylphosphine) dichloride (PdCl2(PPh3)2) and then a pressure of 180 bars is applied with carbon monoxide. The mixture is maintained at 90° C. for 4 days. After cooling and releasing the pressure, a further 3.5 g of PdCl2(PPh3)2 are added, a pressure of 130 bars is applied with carbon monoxide, and the mixture is maintained at 90° C. for 3 days, after which it is cooled to 25° C., the pressure is released and the mixture is discharged. After concentration in vacuo, absorption from ethyl acetate onto silica gel is carried out. The silica gel is applied to a flash chromatography column (silica gel) and then eluted with n-hexanelethyl acetate 3/1. 24.3 g of the desired target compound having a melting point of 48-50° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274536B1
Source datasetuspto-grants-2001_08
ORD IDord-060f7c916bff46c7a17eff68139ff51d
Source noteuspto-grants-2001_08