HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750064Generated: November 1, 2026
Potassium Carbonate → 2-(2-Ethylsulfanyl-4-trifluoromethylsulfanyl-phenyl)-5-trifluoromethylsulfanylbenzoxazole
https://huagongshe.com/reaction/1750064
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-((Trifluoromethyl)sulfinyl)benzo[d]oxazole | HCID 118035497 | — |
| Reactant | 1-Bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene | HCID 118035563 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2-Ethylsulfanyl-4-trifluoromethylsulfanyl-phenyl)-5-trifluoromethylsulfanylbenzoxazole | HCID 118035389 | 15.5% |
Reaction Steps
A mixture of 0.10 g of 5-trifluoromethylsulfinylbenzoxazole, 0.15 g of 1-bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene, 0.01 g of palladium(II) acetate, 0.01 g of triphenylphosphine, 0.02 g of copper(II) acetate monohydrate, 0.13 g of potassium carbonate and 3 ml of toluene was stirred under heating and refluxing for 2 hours. Ethyl acetate and water were added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate and then dried with anhydrous sodium sulfate. The residue obtained by concentrating the mixture under reduced pressure was applied to a silica gel column chromatography to obtain 0.03 g of 2-(2-ethylsulfanyl-4-trifluoromethylsulfanyl-phenyl)-5-trifluoromethylsulfanylbenzoxazole (hereinafter, referred to as Compound 19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156838B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-17ceabe3a46947c0ab7d1dbbe3b97cd2 |
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| Source note | uspto-grants-2015_10 |
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