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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731203Generated: October 27, 2026

Trifluoroacetic acid → Ethyl 3-(4-hydroxyphenyl)-3-(oxazol-5-yl)propanoate

https://huagongshe.com/reaction/731203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-(oxazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylateHCID 68684918—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(4-hydroxyphenyl)-3-(oxazol-5-yl)propanoateHCID 5783579835.7%

Reaction Steps

TFA (10 mL) was added to a solution of 75.3 (14 mmol) in dry DCM (100 mL) and stirred at room temperature for 2 hours. To the reaction mixture was slowly added solid NaHCO3 with stirring. The reaction was then washed with saturated NaHCO3 (2×), dried over Na2SO4, and concentrated under reduced pressure. The residue was then re-dissolved in EtOH, stirred with Pd—C (1.48 g, 0.7 mmol) under hydrogen at room temperature for 14 hours. The Pd—C was removed by filtration through celite with EtOAc as eluant. After concentration, the residue was chromatographed (silica gel, 1:1 EtOAc/hexane) to afford compound 75.4 (1.3 g, 5 mmol). MS ESI (pos.) m/e 262.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582803B2
Source datasetuspto-grants-2009_09
ORD IDord-700ab63c583e4a4985796ecaccb0fc76
Source noteuspto-grants-2009_09