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HRID 9558作成日:2026年10月24日

Sodium Carbonate → 1-(3-Methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanone

https://huagongshe.com/ja/reaction/9558

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1,4-DioxaneHCID 31275—
反応物4-Nitrophenylboronic acidHCID 2773552—
反応物4-Acetyl-3-methylphenyl trifluoromethanesulfonateHCID 11482935—
溶媒TolueneHCID 1140—
生成物1-(3-Methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanoneHCID 2198579899.9%

反応条件

温度85 °C

反応手順

A mixture of 4-acetyl-3-methylphenyl trifluoromethanesulfonate (6.90 g, 24.0 mmol), 4-nitrophenylboronic acid (3.80 g, 24 mmol), 2 N aqueous sodium carbonate (88.0 mL), dioxane (88.0 mL), and toluene (296 mL) was purged with argon for 30 minutes before [1,1′-bis(diphenyl-phosphino)-ferrocene]dichloro palladium(II) (1:1 complex with dichloromethane, 1.90 g, 2.30 mmol) was added. The reaction mixture was heated at 85° C. and stirred overnight. The layers were separated and the organic layer was washed with water (2×50 mL), dried over magnesium sulfate, and concentrated under reduced pressure to give a dark brown oil. This material was purified by flash chromatography (7 to 20% ethyl acetate/hexane) to give 1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone as a light yellow solid (6.12 g, 99% yield). GC-MS m/z 255 (M+), ret. time 9.89 min; 1H NMR (CDCl3) δ: 2.61 (s, 3H), 2.62 (s, 3H), 7.49–55 (m, 2H), 7.78 (d, 2H), 7.81 (d, 1H), 8.32 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091228B2
出典データセットuspto-grants-2006_08
ORD IDord-4b8faee746e147b69f20751ab4e1c852
出典メモuspto-grants-2006_08