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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486376Generated: October 25, 2026

Potassium Carbonate → 9-(4-(8-bromodibenzo[b,d]furan-2-yl)phenyl)-9H-carbazole

https://huagongshe.com/reaction/1486376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant2,8-DibromodibenzofuranHCID 82290—
Reactant9-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazoleHCID 11850073—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Product9-(4-(8-bromodibenzo[b,d]furan-2-yl)phenyl)-9H-carbazoleHCID 11760725370.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of Compound 11 (2.00 g, 4.56 mmol), 2,8-dibromodibenzo[b,d]furan (2.60 g, 7.98 mmol), tetrakis(triphenylphosphine) palladium(0) (0.26 g, 0.23 mmol), potassium carbonate (1.892 g, 13.70 mmol), 1,4-dioxane (60.00 mL), and water (12.00 mL) was degassed with bubbling argon for 1 hour. The reaction mixture was then heated to 80° C. and was stirred overnight (16.5 hours), maintaining an argon atmosphere. Consumption of the starting material was confirmed by thin-layer chromatography and the reaction was cooled to room temperature. The product was extracted with dichloromethane, dried, and purified by silica gel column chromatography with dichloromethane in hexanes as the eluent. The product fractions were then dried and the product was collected to yield Compound 13 (1.57 g, 70%). Confirmed by LCMS (APCI): calculated for C30H18BrNO (M+H): 488. Found: 488.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09425408B2
Source datasetuspto-grants-2016_08
ORD IDord-4a6647a0dcde4912a868e38fb57a2e91
Source noteuspto-grants-2016_08