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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485068Generated: October 31, 2026

Hydrochloric Acid → 4-(1,1-Difluoroethyl)benzaldehyde

https://huagongshe.com/reaction/1485068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant1-Bromo-4-(1,1-difluoroethyl)benzeneHCID 45158847—
SolventTetrahydrofuranHCID 8028—
SolventButyllithiumHCID 178418339—
Product4-(1,1-Difluoroethyl)benzaldehydeHCID 20387577—

Reaction Steps

To a solution of 1-bromo-4-(1,1-difluoroethyl)benzene (1.00 g) in tetrahydrofuran (10.0 mL), n-butyl lithium (2.69 mol/L, solution in n-hexane, 1.68 mL) was added at −80° C. and the mixture was stirred at that temperature for 5 minutes. Subsequently, N,N-dimethylformamide (0.522 mL) was added at −80° C. and after stirring the mixture at that temperature for 20 minutes, 2 mol/L hydrochloric acid (2.50 mL) was added. After bringing the reaction mixture to room temperature, two extractions were conducted with ethyl acetate and the combined organic layers were washed with water. After drying over anhydrous magnesium sulfate and the desiccant was removed by filtration; the filtrate was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-90:10) to give the titled compound as a colorless oil (510 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-e0350786af7147eab5fffba7ba6000bb
Source noteuspto-grants-2016_08