HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233295Generated: October 30, 2026
(Trifluoromethyl)trimethylsilane → HCID 59295451, compound
https://huagongshe.com/reaction/2233295
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 59295400 | HCID 59295400 | — |
| Reactant | HCID 59295476 | HCID 59295476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59295451 | HCID 59295451 | — |
Reaction Steps
To an ice cooled solution of 2.0 g 4-Methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazole-5-carbaldehyde (derived from [4-Methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-methanol according to the method described for 4-Methyl-2-(trans-1,4-trifluoromethyl-cyclohexyl)-thiazole-5-carbaldehyde) and 1.09 ml (trifluoromethyl)trimethylsilane in 10 ml tetrahydrofuran were added 100 mg tetrabutylammoniumfluoride. The reaction mixture was stirred at room temperature for thirty minutes. Then 20 ml 2N HCL were added and the mixture stirred at room temperature for thirty minutes. The mixture was extracted three times with portions of 50 ml ethyl acetate. The combined organic layers were dried over MgSO4. The solvent was evaporated in vacuo to obtain 1.5 g 2,2,2-Trifluoro-1-[4-methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-ethanol as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709481B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-6cb903c0da5d4eefa0d58a6e2d9ec3e3 |
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| Source note | uspto-grants-2010_05 |
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