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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901760Generated: October 26, 2026

Toluene → 2-Phenylanthraquinone

https://huagongshe.com/reaction/901760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-ChloroanthraquinoneHCID 8553—
ReactantPhenylboronic AcidHCID 66827—
ReactantPotassium FluorideHCID 522689—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product2-PhenylanthraquinoneHCID 31399587.1%

Reaction Steps

Under an atmosphere of argon, 2-chloroanthraquinone (5.0 g, 21 mmole), phenylboronic acid (2.8 g, 23 mmole, 1.1 eq), tris(dibenzylidene-acetone)dipalladium(0) (0.2 g, 0.22 mmole, 2% Pd) and potassium fluoride (4.4 g, 76 mmole, 3.3 eq) were suspended in anhydrous dioxane (30 ml). To the obtained suspension, a toluene solution of tri-t-butylphosphine (66%, 0.13 ml, 0.42 mmole, 1 eq) was added and the resultant mixture was stirred at 80° C. for 3 hours. The reaction mixture was filtered and washed with toluene (100 ml). The filtrate was washed with a saturated aqueous solution of sodium chloride (30 ml) and dried with magnesium sulfate. Then, the solvent was removed by distillation and a yellow solid was obtained. The obtained solid was washed with boiling ethanol (50 ml) and a yellow solid (5.2 g, 87%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361796B2
Source datasetuspto-grants-2008_04
ORD IDord-5ccd4908694b4bceb25de6b6e78070b5
Source noteuspto-grants-2008_04