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HRID 7689作成日:2026年10月23日

Potassium Carbonate → 5'-(1,3-Benzoxazol-2-yl)-2'-methyl-1,1'-biphenyl-3-carbonitrile

https://huagongshe.com/ja/reaction/7689

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物TriphenylphosphineHCID 11776—
反応物3-Cyanophenylboronic acidHCID 2734325—
反応物2-(3-Bromo-4-methylphenyl)-1,3-benzoxazoleHCID 21990996—
触媒HCID 178418476HCID 178418476—
溶媒Water 1,2-dimethoxyethaneHCID 18180031—
生成物5'-(1,3-Benzoxazol-2-yl)-2'-methyl-1,1'-biphenyl-3-carbonitrileHCID 21990975—

反応条件

温度80 °C

反応手順

A mixture of 3-cyano-phenylboronic acid (183 mg, 1.3 mmol), 2-(3-bromo-4-methylphenyl)-1,3-benzoxazole (300 mg, 1.04 mmol), dichlorobis(triphenylphosphine)palladium(II) (36.5 mg, 0.052 mmol), triphenylphosphine (27 mg, 0.104 mmol), and potassium carbonate (287 mg, 2.08 mmol) in degassed DME/H2O (5:1, 18 mL) was heated to 80° C. for 18 h. The mixture was cooled to rt and the two layers were separated and the aqueous layer was extracted with EtOAc (3×). The organics were combined, dried over Na2SO4, and evaporated to dryness to give a clear solid. Purification of the crude by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 30 min: 0 to 20% EtOAc) afforded 5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-ddda68329a1d47baa4ac6fb0eabd16f4
出典メモuspto-grants-2006_08