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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650476Generated: October 25, 2026

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

https://huagongshe.com/reaction/650476

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

Temperature110 °C

Reaction Steps

An autoclave is charged with 200 g of 2,3-dichloro-5-trifluoromethylpyridine, 1.85 liters of ethanol, 260 ml of triethylamine and 6.5 g of palladium bis(triphenylphosphine) dichloride (PdCl2(PPh3)2). At 25° C. a pressure of 110 bars is then applied with carbon monoxide and the mixture is maintained 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 of 0.035 mbar. 200 g of the desired product are obtained in the form of a yellow oil having a boiling point of 67-70° C./0.035 mbar (yield 85% of the theoretical yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274536B1
Source datasetuspto-grants-2001_08
ORD IDord-046dd745272d4d8daefffc6dca8299b2
Source noteuspto-grants-2001_08