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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389769Generated: October 25, 2026

1,2-Dichloroethane → 5-(4-(2-Chloroethoxy)phenyl)-2-(2,6-difluorophenyl)oxazole-4-carboxamide

https://huagongshe.com/reaction/389769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2,6-Difluorophenyl)-5-(4-hydroxyphenyl)oxazole-4-carboxamideHCID 59587578—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-(4-(2-Chloroethoxy)phenyl)-2-(2,6-difluorophenyl)oxazole-4-carboxamideHCID 5958737592%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 2-(2,6-difluorophenyl)-5-(4-hydroxyphenyl)oxazole-4-carboxamide (0.100 g, 0.316 mmol) in DMF (5 ml) were added potassium carbonate (0.220 g, 1.58 mmol) and 1,2-dichloroethane (0.50 ml, 6.32 mmol). The reaction was heated to 130° C. via microwave irradiation and held at that temperature for 1 hour. The reaction was then diluted with EtOAc, washed with water and brine and dried over Na2SO4 before being concentrated in vacuo. The resulting residue was purified by silica gel flash chromatography using 0-50% EtOAc in hexane as eluant to afford 5-(4-(2-chloroethoxy)phenyl)-2-(2,6-difluorophenyl)oxazole-4-carboxamide (0.11 g, 0.29 mmol, 92%) as a white solid. LCMS (1) 2.25 min; m/z (ES+) 379/381.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-d941bc281b2d46c8b955c0e14a8bf96e
Source noteuspto-grants-2013_02