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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530767Generated: October 25, 2026

Ethanol → 7H-Dibenzo(a,g)carbazole

https://huagongshe.com/reaction/530767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57655345HCID 57655345—
Reactant7-acetyl-12-bromo-7H-dibenzo [a,g]carbazoleHCID 71277894—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product7H-Dibenzo(a,g)carbazoleHCID 9160—

Reaction Steps

Following the above procedure, Suzuki coupling of 3.8 g of 7-acetyl-12-bromo-7H-dibenzo [a,g]carbazole and 2.7 g of (4-benzo[d]thiazol-2-yl) phenylboronic acid were stirred together in 30 ml of toluene. To this was added 0.02 g of tetrakis(triphenylphosphine)palladium, 2.1 g of potassium carbonate and 10 ml of aqueous ethanol were added and refluxed under nitrogen for 6 h. The reaction was quenched with water and the toluene layer was removed and passed through a celite column. The organic layers were combined and then evaporated in a rotary evaporator under vacuum to yield 4.1 g of 7-acetyl-12-[4-benzo[d]thiazol-2-yl) phenyl]-7H-dibenzo[a,g]carbazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353085B2
Source datasetuspto-grants-2016_05
ORD IDord-6cbb5b4bfd664254a9e8b69ce020987c
Source noteuspto-grants-2016_05