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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532560Generated: October 26, 2026

Ethanol → Ethyl 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1532560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
ReactantHCID 178418416HCID 178418416—
CatalystBis(triphenylphosphine)palladium chlorideHCID 84124—
ProductEthyl 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylateHCID 2201355885%

Reaction Conditions

Temperature25 °C

Reaction Steps

An autoclave is loaded with 200 g of 2,3-dichloro-5-trifluoromethylpyridine, 1.85 l of ethanol, 260 ml of triethylamine and 6.5 g of palladium bis(triphenylphosphine)dichloride (PdCl2(PPh3)2). 110 bar of carbon monoxide are then forced in at 25° C. and the mixture is kept at 110° C. for 24 hours. After cooling to 25° C., the crude mixture is concentrated to a thick slurry, which is then partitioned between dilute sodium chloride solution and ethyl acetate. After extraction by shaking and separation of the phases, the ethyl acetate phase is washed with water, dried over sodium sulfate and concentrated to dryness. The crude product is distilled under a high vacuum at 0.035 mbar. 200 g of the desired product are obtained as a yellow oil of boiling point 67-70° C./0.035 mbar (yield 85% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204221B1
Source datasetuspto-grants-2001_03
ORD IDord-d29fa9fbecd24dc2b9ef39ec3d0cf1e9
Source noteuspto-grants-2001_03