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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367818Generated: November 2, 2026

Hydrochloric Acid → 1-(2,4-Difluorophenyl)-2,2,2-trifluoroethan-1-ol

https://huagongshe.com/reaction/1367818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,4-DifluorobenzaldehydeHCID 73770—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
CatalystTetrahydrofuranHCID 8028—
SolventTetrahydrofuranHCID 8028—
Product1-(2,4-Difluorophenyl)-2,2,2-trifluoroethan-1-olHCID 61086802117.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,4-Difluorobenzaldehyde (1.1 mL, 10.0 mmol) and (trifluoromethyl)trimethylsilane (1.77 mL, 12.0 mmol) were dissolved in THF (25 mL) and then cooled to 0° C. To this, 1M TBAF in THF (76 μL, 76 μmol) was added and the reaction mixture was allowed to warm to room temperature. After 3.25 h, 2.5M HCl (25 mL) was added. The reaction was stirred for 1 h and then extracted with ether. The organic layer was washed with brine and dried with Na2SO4. The solvent was removed under the reduced pressure to give 2,2,2-trifluoro-1-(2,4-difluoro-phenyl)ethanol (2.5 g) as a racemic mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893093B2
Source datasetuspto-grants-2011_02
ORD IDord-85b58a424fc4426299e11fe5d2c7df16
Source noteuspto-grants-2011_02