HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854683Generated: October 26, 2026
Potassium Iodide → 1-[2-(4-{2-[(e)-2-(4-Trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1h-[1,2,3]triazole
https://huagongshe.com/reaction/854683
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Chloromethyl-2-[2-(4-trifluoromethyl-phenyl)-vinyl]-thiazole | HCID 69428679 | — |
| Reactant | 4-(4-[1,2,3]Triazol-1-ylmethyl-oxazol-2-yl)-phenol | HCID 136355231 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-[2-(4-{2-[(e)-2-(4-Trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1h-[1,2,3]triazole | HCID 11202994 | 67.1% |
Reaction Steps
A mixture of 0.1212 g (0.50 mmol) 4-(4-[1,2,3]triazol-1-ylmethyl-oxazol-2-yl)-phenol and 0.10 g (0.30 mmol) cesium carbonate in 10 ml butanone was stirred at 60° C. for 30 min, then 0.152 g (0.50 mmol) 4-chloromethyl-2-[2-(4-trifluoromethyl-phenyl)-vinyl]-thiazole and 0.083 g (0.50 mmol) potassium iodide were added and stirring at 60° C. continued over night. After evaporation, 15 ml water was added and the mixture extracted with two portions of 15 ml ethyl acetate. The combined organic layers were washed with 1N sodium hydroxide and water, dried over sodium sulfate and evaporated to give 201 mg raw material which was recrystallised from ethanol to yield 171 mg (67%) 1-[2-(4-{2-[(E)-2-(4-trifluoromethyl-phenyl)-vinyl]-thiazol-4-ylmethoxy}-phenyl)-oxazol-4-ylmethyl]-1H-[1,2,3]triazole as white crystals melting at 179-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259262B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-b1d742f4d56648759057574e28f1270b |
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| Source note | uspto-grants-2007_08 |
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