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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375958Generated: November 5, 2026

Sodium Carbonate → 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-carbaldehyde

https://huagongshe.com/reaction/2375958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
ReactantTrifluoro-methanesulfonic acid 4-(2-benzyl-benzofuran-3-yl)-phenyl esterHCID 59696180—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-carbaldehydeHCID 5985551188%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of the triflate (from example 10) (9.35 g, 21.6 mmol) and tetrakis-(triphenylphosphine)palladium(0) (750 mg, 0.65 mmol) in toluene (70 mL) was added a solution of 4-formylphenylboronic acid (4.06 g, 27.05 mmol) in ethanol (20 mL) and 2N sodium carbonate (21.6 mL, 43.2 mmol). The resulting suspension was stirred at 100° C. for 4 hrs (TLC control). The reaction was cooled, diluted with water (50 mL) and extracted with diethyl ether (3×100 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting brown solid was redissolved in tetrahydrofuran (50 mL). 2N Hydrochloric acid (10 mL) was added and the resulting solution was stirred at room temperature for 1 hour, and then diluted with water (50 mL) and extracted with diethyl ether (3×100 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification of the product by flash column chromatography, using 20% ethyl acetate in heptane as eluent, afforded the title compound as a white solid (7.34 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465825B2
Source datasetuspto-grants-2008_12
ORD IDord-46491a3c516f4f04aa6aca0ed0bfa0c3
Source noteuspto-grants-2008_12