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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533621Generated: October 30, 2026

Triphenylphosphine → 2-(2-Methylsulfanylphenyl)-5-trifluoromethylbenzoxazole

https://huagongshe.com/reaction/533621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantN-(2-hydroxy-5-trifluoromethylphenyl)-2-methylsulfanylbenzamideHCID 67981373—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Methylsulfanylphenyl)-5-trifluoromethylbenzoxazoleHCID 6798207889.8%

Reaction Steps

To a mixture of N-(2-hydroxy-5-trifluoromethylphenyl)-2-methylsulfanylbenzamide (0.33 g), triphenylphosphine (0.34 g), and THF (7 ml), diethyl azodicarboxylate (40% in toluene) (0.57 g) was added dropwise, and stirred at room temperature for 1.5 hours. Triphenylphosphine (79 mg) and diethyl azodicarboxylate (40% in toluene, 0.13 g) were added to the mixture, and stirred for further 1 hour. The mixture was heated to 50° C., and stirred for 1.5 hours. The reaction mixture was cooled to room temperature, and then the mixture was allowed to stand at room temperature overnight. The reaction mixture was subjected to silica gel column chromatography to give 0.28 g of 2-(2-methylsulfanylphenyl)-5-trifluoromethylbenzoxazole (hereinafter referred to as Present Compound 77).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853238B2
Source datasetuspto-grants-2014_10
ORD IDord-3937cd433ae44b7694764f1138f968f7
Source noteuspto-grants-2014_10