HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Trifluoromethyl)trimethylsilane → α-(Trifluoromethyl)-5-thiazolemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 1,3-Thiazole-5-carbaldehyde | HCID 2773577 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | α-(Trifluoromethyl)-5-thiazolemethanol | HCID 67130512 | 68.9% |
Reaction Steps
The method described in Example 4 (step 4.5.) is followed. Starting from 2 g (17.68 mmol) of thiazole-5-carboxaldehyde, 0.88 ml (0.88 mmol) of a 1M solution of tetrabutylammonium fluoride in THF and 2.765 g (19.44 mmol) of trifluoromethyltrimethylsilane (TMS-CF3), and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, gives 2.23 g of pure product in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912218B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-a1024248a7f14ff8b9fd1e47c99a1d84 |
| Source note | uspto-grants-2014_12 |