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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514016Generated: November 3, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 57703127, compound

https://huagongshe.com/reaction/1514016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantPotassiumHCID 5462222—
Reactant9H-3,9'-BicarbazoleHCID 13236022—
Reactant8-Chlorobenzofuro[3,2-b]pyridineHCID 68734215—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
ProductHCID 57703127HCID 5770312750%

Reaction Steps

The 100 mL round bottom flask, equipped with magnetic stirrer and refluxed condenser, was charged with 8-chlorobenzofuro[3,2-b]pyridine (2.04 g, 10 mmol), 3-(9-carbazolyl)carbazole (3.32 g, 10 mmol), Pd(OAc)2 (450 mg, 20 mol %), P(t-Bu)3 (10 mL of 1M solution in toluene, 10 mmol), potassium tert-buthoxide (1.92 g, 1.5 eq) and 150 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 2.5 g of 8-(9H-3,9′-bicarbazol-9-yl)benzofuro[3,2-b]pyridine 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-c21a053752d64d07aa619c4f9a9f9fb5
Source noteuspto-grants-2012_07