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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957899Generated: November 3, 2026

1,3-Dibromobenzene → 1-(3-(3-bromophenyl)-9H-carbazol-9-yl)ethanone

https://huagongshe.com/reaction/1957899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromobenzeneHCID 7927—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazol-9-yl)ethanoneHCID 71236252—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(3-(3-bromophenyl)-9H-carbazol-9-yl)ethanoneHCID 7123639623%

Reaction Steps

A mixture solution of 1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazol-9-yl)ethanone (10.00 g, 29.8 mmol), 1,3-dibromobenzene (17.59 g, 74.6 mmol), Pd(PPh3)4 (0.689 g, 0.597 mmol) and K2CO3 (12.37 g, 89 mmol) in toluene (100 mL) and water (20 mL) was refluxed under N2 overnight. After cooling to room temperature, the organic phase was isolated and the solvent was evaporated. The residue was purified by column chromatography on silica gel with hexane/DCM (1/1, v/v) as eluent to yield 1-(3-(3-bromophenyl)-9H-carbazol-9-yl)ethanone (2.5 g, 23%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08409729B2
Source datasetuspto-grants-2013_04
ORD IDord-fa11a77dab5741409ecc2b3c321447b0
Source noteuspto-grants-2013_04