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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894815Generated: November 1, 2026

Trifluoroacetic acid → HCID 66591104, compound

https://huagongshe.com/reaction/1894815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66591328HCID 66591328—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 66591104HCID 66591104112%

Reaction Steps

A solution of 852 mg (2.23 mmol) of ethyl 3-{6-[3-(tert-butoxycarbonylmethylamino)phenyl}pyrid-3-yl}acrylate in 10 mL of methanol is stirred for 4 hours at room temperature in the presence of 100 mg of 10% palladium-on-charcoal under a hydrogen atmosphere. The catalyst is filtered off and the solvents are then evaporated off. The oil obtained is dissolved in 15 mL of dichloromethane. 2 mL of trifluoroacetic acid are added and the reaction mixture is stirred for 4 hours at room temperature. The reaction is stopped by adding 100 mL of saturated sodium hydrogen carbonate solution and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 710 mg of ethyl 3-[6-(3-methylaminophenyl)pyrid-3-yl]propanoate are obtained. Yield=68%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513297B2
Source datasetuspto-grants-2013_08
ORD IDord-67baa8c43e4f46649911f4845a3ee651
Source noteuspto-grants-2013_08