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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403150Generated: October 27, 2026

9-Acetyl-3-bromocarbazole → HCID 71060157, compound

https://huagongshe.com/reaction/403150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Acetyl-3-bromocarbazoleHCID 1714879—
Reactant(3-(carbazole-9H)Phenyl)Pinacol esterHCID 58690899—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 71060157HCID 7106015794%

Reaction Steps

A solution of 1-(3-bromo-9H-carbazol-9-yl)ethanone (2.000 g, 6.94 mmol), 9-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole (2.56 g, 6.94 mmol), Pd2(dba)3 (0.064 g, 0.069 mmol), SPhos (0.057 g, 0.139 mmol) and potassium phosphate tribasic hydrate (4.80 g, 20.82 mmol) in toluene (100 mL) and water (10 mL) was stirred at 70° C. under nitrogen overnight. After cooling to room temperature, the organic phase was isolated. Upon evaporation of the solvent, the residue was purified by column chromatography on silica gel with hexane:DCM (1:4, v/v) as eluent to yield 1-(3-(3-(9H-carbazol-9-yl)phenyl)-9H-carbazol-9-yl)ethanone (2.9 g, 94%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748012B2
Source datasetuspto-grants-2014_06
ORD IDord-8ff4e04a4c12455c97af41ea10863806
Source noteuspto-grants-2014_06