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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525977Generated: October 23, 2026

Ethanol → HCID 68441434, compound

https://huagongshe.com/en/reaction/525977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3,6-DibromocarbazoleHCID 274874—
ReactantSodium BicarbonateHCID 516892—
Reactant4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 68441434HCID 68441434—

Reaction Conditions

Temperature90 °C

Reaction Steps

3,6-dibromocarbazole (3.03 g, 9.32 mmol), 4-(octyloxy)phenylboronic acid (7.14 g, 28.5 mmol), aqueous NaHCO3 (80 ml), ethanol (120 ml) and toluene (190 ml) was mixed and degassed with nitrogen for 15 minutes before adding the Pd(PPh3)4 catalyst (80 mg, 0.07 mmol). The reaction mixture was then brought to reflux at 90° C. for 5 h 20 minutes. It was quenched with water when reached room temperature and extracted three times with ethyl acetate. The combined organic phases were washed with brine and water and evaporated. The residual solid was dissolved in toluene and precipitated in petroleum ether. The precipitate was purified using column chromatography with toluene as mobile phase which yielded 3,6-bis(4-(octyloxy)phenyl)-carbazole (5.42 g, 9.41 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09343198B2
Source datasetuspto-grants-2016_05
ORD IDord-17a430f12f94472fb301a45aff739f46
Source noteuspto-grants-2016_05