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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 9H-3,9'-Bicarbazole | HCID 13236022 | — |
| Reactant | 8-Chlorobenzofuro[3,2-b]pyridine | HCID 68734215 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 57703127 | HCID 57703127 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08221905B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-c21a053752d64d07aa619c4f9a9f9fb5 |
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| Source note | uspto-grants-2012_07 |
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