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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714979Generated: October 29, 2026

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

https://huagongshe.com/reaction/714979

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 numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-1e0749de3f044e54a9fccc581cebc191
Source noteuspto-grants-2015_11