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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205148Generated: November 1, 2026

Potassium Phosphate, Tribasic → HCID 86718133, compound

https://huagongshe.com/reaction/2205148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantMethyl 3-bromo-2-phenylquinoxaline-6-carboxylateHCID 86667202—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86718133HCID 86718133—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09370522B2
Source datasetuspto-grants-2016_06
ORD IDord-8cce260cb03b439bac093d47f56b99aa
Source noteuspto-grants-2016_06