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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782669Generated: October 30, 2026

Potassium Carbonate → HCID 59655978, compound

https://huagongshe.com/reaction/1782669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSilane, (4-bromophenyl)trimethyl-HCID 138897—
ReactantDibenzofuran-4-boronic acidHCID 2734328—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 59655978HCID 5965597896.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of dibenzofuran-4-yl-boronic acid (20.0 g, 94.3 mmol), (4-bromo-phenyl)-trimethyl-silane (21.62 g, 94.3 mmol), K2CO3 (39.1 g, 3 equiv., 283 mmol) in toluene (100 mL), ethanol (60 mL) and water (30 mL) was purged with nitrogen for 5 min (bubbled into solution) and treated with Pd(PPh3)4 (3.59 g, 2.9 mmol). After heating to 80° C. for 4 h, the solution was cooled to room temperature, poured into water (300 mL) and extracted with ethyl acetate (300 mL). The organic phase was washed with sat'd aq NaCl, dried over anhydrous MgSO4 , filtered and concentrated in vacuo. Purification by flash column chromatography (5-20% ethyl acetate in heptane) afforded (4-dibenzofuran-4-yl-phenyl)-trimethyl-silane as a colorless oil (28.9 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498356B2
Source datasetuspto-grants-2009_03
ORD IDord-101023113fe040809a5c82f0e36ff349
Source noteuspto-grants-2009_03