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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716856Generated: November 2, 2026

Potassium Carbonate → Ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/1716856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
ReactantEthyl 2-chlorooxazole-4-carboxylateHCID 2763184—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylateHCID 4683478970%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of ethyl 2-chloro-1,3-oxazole-4-carboxylate (0.59 g, 3.36 mmol) in dioxane was treated with 4-(hydroxymethyl)phenyl boronic acid (0.766 g, 5.04 mmol), K2CO3 (0.929 g, 6.72 mmol), t-Bu3PhBF4 (0.049 g, 0.168 mmol) heated to 80° C. then treated with Pd2(dba)3 (0.154 g 0.168 mmol) and stirred overnight at 90° C. The reaction mixture was diluted with EtOAc, washed with water, saturated sodium chloride, dried over MgSO4 and concentrated in in vacuo. The resultant residue was purified by flash chromatography (silica, EtOAc:hexanes 20→50%) to give the title product in 70% yield, identified by NMR and mass spectral analyses. LCMS (ESI+) 248 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803825B2
Source datasetuspto-grants-2010_09
ORD IDord-5480ed18099c49f081b718c2ece56031
Source noteuspto-grants-2010_09