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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389746Generated: October 27, 2026

Stannane, hydroxytrimethyl- → 2-(2,6-Difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acid

https://huagongshe.com/reaction/389746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, hydroxytrimethyl-HCID 11217597—
ReactantEthyl 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylateHCID 59587399—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product2-(2,6-Difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acidHCID 5958754341.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylate (0.080 g, 0.23 mmol) in DCE (8 mL) was added trimethyltin hydroxide (0.300 g, 1.66 mmol) and the resulting solution stirred at 80° C. overnight. A further portion of trimethyltin hydroxide (0.168 g, 0.93 mmol) was added and the solution stirred at 80° C. overnight. The reaction was diluted with DCM and washed with 1M aqueous HCl and brine. The organic phase was dried over MgSO4 and solvent removed in vacuo. The residue was purified by silica gel column chromatography using an 8% to 50% EtOAc in hexanes gradient followed by a 5% to 50% MeOH in DCM gradient to afford 2-(2,6-difluorophenyl)-5-(phenylamino)oxazole-4-carboxylic acid (0.030 g, 0.095 mmol, 41% three steps). LCMS (1) Rt: 1.46 min; m/z (ES+) 317.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-0e80ec1c7f544c14b77a1facd41a8dc8
Source noteuspto-grants-2013_02