HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205148Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 86718133, compound
https://huagongshe.com/reaction/2205148
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | Methyl 3-bromo-2-phenylquinoxaline-6-carboxylate | HCID 86667202 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86718133 | HCID 86718133 | — |
Reaction Steps
Into a 10-mL sealed tube purged and maintained with an inert atmosphere of nitrogen, was placed a solution of methyl 3-bromo-2-phenylquinoxaline-6-carboxylate (200 mg, 0.58 mmol, 1.00 equiv) in 1,4-dioxane (3 mL). To this was added 4-methoxyphenylboronic acid (133 mg, 0.88 mmol, 1.50 equiv). Addition of Pd2(dba)3 (32 mg, 0.03 mmol, 0.06 equiv) was next. This was followed by the addition of PCy3 (22 mg, 0.08 mmol, 0.14 equiv). To the mixture was added K3PO4 (330 mg, 1.56 mmol, 3.00 equiv). The resulting solution was allowed to react, with stifling, overnight while the temperature was maintained at 110° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:50). This resulted in 160 mg (74%) of methyl 3-(4-methoxyphenyl)-2-phenylquinoxaline-6-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09370522B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-8cce260cb03b439bac093d47f56b99aa |
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| Source note | uspto-grants-2016_06 |
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