HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201374Generated: October 29, 2026
Triphenylphosphine → HCID 117988838, compound
https://huagongshe.com/reaction/2201374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Bis(2-methoxyethyl) diazene-1,2-dicarboxylate | HCID 22836032 | — |
| Reactant | HCID 117998109 | HCID 117998109 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117988838 | HCID 117988838 | 75% |
Reaction Steps
A mixture of 2.13 g of 2-ethylsulfanyl-N-[2-hydroxy-5-(trifluoromethylsulfanyl)phenyl]nicotinamide, 2.14 g of DMEAD, 2.24 g of triphenylphosphine and 20 ml of THF was stirred at 50° C. for 4 hours. A saturated aqueous ammonium chloride solution was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 1.52 g of 2-(2-ethylsulfanylpyridin-3-yl)-5-(trifluoromethylsulfanyl)benzoxazole (hereinafter, referred to as Compound of Present Invention 38).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09364000B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-a6f3dfe2c12d42cba3509bce5b7a493f |
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| Source note | uspto-grants-2016_06 |
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