戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 901760作成日:2026年10月26日

Toluene → 2-Phenylanthraquinone

https://huagongshe.com/reaction/901760

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-ChloroanthraquinoneHCID 8553—
反応物Phenylboronic AcidHCID 66827—
反応物Potassium FluorideHCID 522689—
触媒Tris(1,1-dimethylethyl)phosphineHCID 83681—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物2-PhenylanthraquinoneHCID 31399587.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361796B2
出典データセットuspto-grants-2008_04
ORD IDord-5ccd4908694b4bceb25de6b6e78070b5
出典メモuspto-grants-2008_04