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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277300Generated: October 31, 2026

Ethanol → Ethyl 3-fluoro-5-hydroxypicolinate

https://huagongshe.com/reaction/2277300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant5-((Tert-butyl(diphenyl)silyl)oxy)-2-chloro-3-fluoropyridineHCID 86731381—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductEthyl 3-fluoro-5-hydroxypicolinateHCID 86731382—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-((tert-butyl(diphenyl)silyl)oxy)-2-chloro-3-fluoropyridine (29.5 g), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride (5.59 g), triethylamine (10.7 mL), ethanol (300 mL) and DMF (300 mL) was stirred overnight at 80° C. under a carbon monoxide atmosphere. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The combined organic layer were washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (30.8 g) as a mixture with DMF.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-6e9241dba6cc43e586c897bb30a657cd
Source noteuspto-grants-2015_09