HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533621Generated: October 30, 2026
Triphenylphosphine → 2-(2-Methylsulfanylphenyl)-5-trifluoromethylbenzoxazole
https://huagongshe.com/reaction/533621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | N-(2-hydroxy-5-trifluoromethylphenyl)-2-methylsulfanylbenzamide | HCID 67981373 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Methylsulfanylphenyl)-5-trifluoromethylbenzoxazole | HCID 67982078 | 89.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853238B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3937cd433ae44b7694764f1138f968f7 |
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| Source note | uspto-grants-2014_10 |
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