HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717996Generated: October 31, 2026
Potassium Phosphate, Tribasic → HCID 86684645, compound
https://huagongshe.com/reaction/717996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane | HCID 10997426 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | HCID 86684646 | HCID 86684646 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86684645 | HCID 86684645 | 60.1% |
Reaction Steps
4-chloro-2-(6-isopropyldibenzo[b,d]furan-4-yl)pyridine (10.5 g, 32.6 mmol) and potassium phosphate (22.54 g, 98 mmol) were dissolved in 500 mL of toluene and 50 mL of water. The reaction was purged with nitrogen for 20 minutes and then 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (6.13 mL, 32.6 mmol), Pd2(dba)3 (0.598 g, 0.653 mmol) and dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (1.072 g, 2.61 mmol) were added. The reaction was refluxed for 18 hours. After cooling the reaction to room temperature, 100 mL of water was added to the reaction mixture. The aqueous layer was extracted twice with 100 mL of ethyl acetate. The organic layer was passed through a plug of silica gel, eluting with DCM. After evaporation of the solvent, the crude product was subjected to column chromatography (SiO2, 3% ethyl acetate in hexane to 5% ethyl acetate in hexane, v/v) to yield 6.3 g (60.1%) of pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193745B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-dae90798834643da8e33b67b7ebe1209 |
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| Source note | uspto-grants-2015_11 |
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