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HRID 381835作成日:2026年10月25日

Sodium Carbonate → 4-(4'-Methyl-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester

https://huagongshe.com/reaction/381835

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Tolylboronic acidHCID 79799—
反応物Methyl 4-(4-bromophenyl)-4-oxobutanoateHCID 838865—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物4-(4'-Methyl-biphenyl-4-yl)-4-oxo-butyric acid, methyl esterHCID 7021156369.4%

反応手順

To a stirred mixture of (4-methylphenyl)boronic acid (0.818 g, 0.00602 mol) and 4-(4-bromo-phenyl)-4-oxo-butyric acid, methyl ester (1.3556 g, 0.00500 mol) in toluene (10 mL) was added tetrakis(triphenylphosphine)-palladium(0) (0.173 g, 0.000150 mol) and 2.0 M aqueous sodium carbonate (5.0 mL, 0.010 mol), and the mixture was heated at reflux under nitrogen for 12 hours and allowed to cool. The mixture was diluted with toluene and dichloromethane (10 mL/10 mL), and filtered through a pad of Celite. The Celite was washed with additional toluene and dichloromethane. Filtrate and washings were combined and washed with 2.0 M aqueous sodium carbonate, brine, 3% aqueous ammonium hydroxide, water, and brine. The organics were dried (Na2SO4) and rotary evaporated. The residue was dissolved in chloroform and purified by column chromatography on silica gel (144 g, 230-400 mesh), eluting with hexanes-acetone (6:1, 17×125 mL) to give 0.98 g of 4-(4′-methyl-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a white solid; mp 121-122° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06307089B2
出典データセットuspto-grants-2001_10
ORD IDord-e1ad33f04f7945c9b86aacb99e319450
出典メモuspto-grants-2001_10