Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177656Generated: October 29, 2026

Water → 9-(3-Bromophenyl)-9H-carbazole

https://huagongshe.com/reaction/2177656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbazoleHCID 6854—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-bromo-3-iodo-HCID 11561—
CatalystCopperHCID 23978—
SolventDichloromethaneHCID 6344—
SolventDichloromethane cyclohexaneHCID 21916607—
Product9-(3-Bromophenyl)-9H-carbazoleHCID 5869088882.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

Under nitrogen, carbazole (24.3 g, 1 eq.) is added to a flask together with 1-bromo-3-iodobenzene (98%; 75.3 g, 1.9 eq.), potassium carbonate (48.2 g, 2.5 eq.) and copper (1.77 g, 0.1 eq.). The reaction is heated to 150° C. and stirred at 150° C. for 48 h. The mixture is cooled to room temperature and diluted with 150 mL of methylene chloride. 100 mL of demineralized water are added to the mixture, which is stirred. Removal of the aqueous phase is followed by washing a further 2× with demineralized water (100 mL). The organic phase is dried over sodium sulfate and concentrated. The excess 1-bromo-3-iodobenzene is distilled off under reduced pressure. LC (SiO2; cyclohexane/methylene chloride 95:5) gives 37.1 g of product (82.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067919B2
Source datasetuspto-grants-2015_06
ORD IDord-2b5d18e84d704e6ab53ff9e2691e344b
Source noteuspto-grants-2015_06