Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514010Generated: November 3, 2026

Tris(1,1-dimethylethyl)phosphine → 9-(dibenzo[b,d]furan-2-yl)-9H-3,9'-bicarbazole

https://huagongshe.com/reaction/1514010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassiumHCID 5462222—
Reactant9H-3,9'-BicarbazoleHCID 13236022—
Reactant8-Iodo-3,4-dihydrodibenzo[b,d]furanHCID 68735608—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product9-(dibenzo[b,d]furan-2-yl)-9H-3,9'-bicarbazoleHCID 5770316682.2%

Reaction Steps

The 100 mL round bottom flask, equipped with magnetic stirrer and refluxed condenser, was charged with 8-iodo-3,4-dihydrodibenzo[b,d]furan (332 mg, 1 mmol), 3-(9-carbazolyl)carbazole (294 mg, 1 mmol), Pd(OAc)2 (23 mg, 10 mol %), P(t-Bu)3 (1 mL of 1M solution in toluene, 1 mmol), potassium tert-buthoxide (150 mg, 1.5 eq) and 100 ml of xylene. The flask was filled with nitrogen, and the reaction mixture was heated to reflux and stirred under nitrogen atmosphere for 24 hours. Then reaction was cooled down to room temperature, filtered through silica plug and evaporated. The residue was subjected to column chromatography on silica gel, eluent hexane/ethyl acetate mixture 9:1, providing 410 mg of 9-(dibenzo[b,d]furan-2-yl)-9H-3,9′-bicarbazole as white solid. The structure was confirmed by NMR and MS spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08221905B2
Source datasetuspto-grants-2012_07
ORD IDord-21bb7b40c6134599bfc49bf680235ae9
Source noteuspto-grants-2012_07