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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669241Generated: October 31, 2026

Potassium Carbonate → 4'-(Trifluoromethyl)-4-biphenylcarbaldehyde

https://huagongshe.com/reaction/1669241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product4'-(Trifluoromethyl)-4-biphenylcarbaldehydeHCID 278271299.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To an ambient temperature solution of 4-(trifluoromethyl)phenylboronic acid (4.64 g, 24.43 mmol) in dioxane/water (15/15 mL) is added 4-bromo-benzaldehyde (4.42 g, 22.21 mmol), tetrabutylammonium bromide (7.16 g, 22.21 mmol, potassium carbonate (7.67 g, 55.53 mmol) and degassed for 10 min. Palladium(II) acetate (748 mg, 1.11 mmol) is added and the reaction mixture is heated to 70° C. After 2 h TLC (20% EtOAc/hexane) indicates complete consumption of starting material. The reaction is cooled to room temperature diluted with water and extracted with EtOAc (3×200 mL). The combined organic extracts are washed with brine, dried (MgSO4), filtered, concentrated and chromatographed (330 g SiO2, 5% EtOAc/Hexanes) to yield the title compound (5.54 g, 94%). 1NMR (400 MHz, CDCl3) δppm: 10.09 (s, 1H), 8.01-8.00 (m, 1H), 7.99-7.98 (m, 1H), 7.78-7.75 (m, 2H), 7.74 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-dee379efd5bb4446a9feb63bf0f3366a
Source noteuspto-grants-2011_08