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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516493Generated: October 26, 2026

Potassium Carbonate → 3-(4-Bromophenyl)-9-phenylcarbazole

https://huagongshe.com/reaction/516493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazoleHCID 57415695—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product3-(4-Bromophenyl)-9-phenylcarbazoleHCID 5135829344%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (Compound 14) (5.0 g, 13.5 mmol), 4-bromoiodobenzene (10.76 g, 38 mmol), Pd(PPh3)4 (0.5 g, 0.43 mmol) and potassium carbonate (K2CO3)(5.52 g, 40 mmol) in dioxane/water (80 mL/15 mL) was degassed and heated at about 100° C. overnight, then worked up with ethyl acetate/brine. The organic phase was collected, dried over Na2SO4, and purified by flash column (hexanes to hexane/ethyl acetate 90:1). The main fraction was collected, concentrated, and a precipitate was filtered to give a white solid (Compound 15) (2.35 g, in 44% yield). Confirmed by LCMS (APCI): calculated for C24H17BrN (M+H): 398; Found: 398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09112159B2
Source datasetuspto-grants-2015_08
ORD IDord-51241983bc27482185fe02ffef621da1
Source noteuspto-grants-2015_08