Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403694Generated: October 30, 2026

(Trifluoromethyl)trimethylsilane → α-(Trifluoromethyl)-5-thiazolemethanol

https://huagongshe.com/reaction/1403694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1,3-Thiazole-5-carbaldehydeHCID 2773577—
SolventTetrahydrofuranHCID 8028—
Productα-(Trifluoromethyl)-5-thiazolemethanolHCID 6713051268.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912218B2
Source datasetuspto-grants-2014_12
ORD IDord-a1024248a7f14ff8b9fd1e47c99a1d84
Source noteuspto-grants-2014_12