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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254738Generated: October 25, 2026

Hydrochloric Acid → 2,2,2-Trifluoro-1-[2-(trifluoromethyl)phenyl]ethan-1-ol

https://huagongshe.com/reaction/254738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanto-(Trifluoromethyl)benzaldehydeHCID 123067—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trifluoro-1-[2-(trifluoromethyl)phenyl]ethan-1-olHCID 6164499390.1%

Reaction Steps

Tetrabutylammonium fluoride (0.1 ml; 1.0 M solution in tetrahydrofuran) was added to a solution of 2-trifluoromethyl-benzaldehyde (1.74 g, 10 mmol) and trifluoromethyltrimethylsilane (TMSCF3) (1.8 ml, 12 mmol) in 10 ml THF at 0° C. The formed mixture was warmed up to room temperature and stirred for 4 hours. The reaction mixture was then treated with 12 ml of 1N HCl and stirred overnight. The product was extracted with ethyl acetate (3×20 ml). The organic layer was separated and dried over sodium sulfate. The organic solvent was evaporated to give 2.2 g of 1-(2-trifluoromethylphenyl)-2,2,2-trifluoro-ethanol, yield 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875622B2
Source datasetuspto-grants-2011_01
ORD IDord-50bc8270d04f4fcebda9df5f3a8fd71e
Source noteuspto-grants-2011_01