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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499126Generated: November 2, 2026

Hydrochloric Acid → 1-(5-Bromo-[1,1'-biphenyl]-2-yl)-2,2,2-trifluoroethanol

https://huagongshe.com/reaction/1499126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-Bromo-[1,1'-biphenyl]-2-carbaldehydeHCID 54197319—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Bromo-[1,1'-biphenyl]-2-yl)-2,2,2-trifluoroethanolHCID 117942108—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-bromo-[1,1′-biphenyl]-2-carbaldehyde (1.9 g, 7.3 mmol) and was added TMSCF3 (1.2 g, 8.7 mmol) in THF (20 mL) and cooled to 0° C. To this solution was added TBAF (1.46 mL, 1M in THF) and the reaction mixture was warmed to RT for 3 h. After this time, the mixture was treated with 3 N HCl (5 mL) and stirred for 12 h. Then the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered, concentrated in vacuo and purified by normal phase silica gel column (EtOAc:PE=1:10) to afford 1-(5-bromo-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-8f7da66d5a9548858237e03e2a8ca154
Source noteuspto-grants-2015_12