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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642328Generated: November 1, 2026

Phenyl dihydrogen orthoborate → HCID 57514566, compound

https://huagongshe.com/reaction/1642328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl dihydrogen orthoborateHCID 78412—
ReactantQuinoxaline, 5-bromo-7-methyl- (9CI)HCID 45117463—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventSodium CarbonateHCID 10340—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57514566HCID 57514566—

Reaction Steps

A mixture of 400 mg of 5-bromo-7-methyl-quinoxaline, 244 mg of phenylboric acid and 100 mg of tetrakis(triphenylphosphine)palladium in 12 ml dioxane, 4 ml of methanol and 3.6 ml 1 M aqueous sodium carbonate solution is refluxed for three hours under an argon atmosphere. Then the reaction mixture is evaporated down and the residue is distributed between ethyl acetate and water. The ethyl acetate phase is separated off, dried over magnesium sulphate and evaporated down. The crude product is purified by chromatography over a silica gel column with cyclohexane/ethyl acetate (85:15 to 70:30) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119648B2
Source datasetuspto-grants-2012_02
ORD IDord-0397107e82a04046963fd8f4b1dde079
Source noteuspto-grants-2012_02