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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400009Generated: November 4, 2026

Hydrochloric Acid → 1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethanol

https://huagongshe.com/reaction/1400009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromo-2-fluorobenzaldehydeHCID 143517—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-2-fluorophenyl)-2,2,2-trifluoroethanolHCID 6164463598%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-bromo-2-fluoro-benzaldehyde (8.12 g, 40.0 mmol) and (trifluoromethyl)trimethylsilane (7.50 mL, 48.0 mmol) in THF (40 mL) was cooled to 0° C. before treating with TBAF (1 M in THF, 0.6 mL) and warming to rt. After 3 h, an additional portion of TBAF (1 M in THF, 8.0 mL) was added. The resultant mixture was allowed to stir for 10 min before adding HCl (1 N aq., 40 mL) and extracting with Et2O (40 mL). The Et2O layer was dried (MgSO4) and concentrated to yield the title compound (10.7 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906914B2
Source datasetuspto-grants-2014_12
ORD IDord-b9623235aa6e4b86907322ddde276ceb
Source noteuspto-grants-2014_12