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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 381835Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/381835

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTolylboronic acidHCID 79799—
EduktMethyl 4-(4-bromophenyl)-4-oxobutanoateHCID 838865—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4'-Methyl-biphenyl-4-yl)-4-oxo-butyric acid, methyl esterHCID 7021156369,4%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06307089B2
Quelldatensatzuspto-grants-2001_10
ORD IDord-e1ad33f04f7945c9b86aacb99e319450
Quellennotizuspto-grants-2001_10