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HRID 537337Erstellt: 25. Oktober 2026

Potassium Phosphate, Tribasic → 3-[3-(4-Chlorophenyl)-6-methylphenyl]-5,5-dimethylpyrrolidine-2,4-dione

https://huagongshe.com/reaction/537337

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-(Di-tert-butylphosphino)-2'-methyl-1,1'-biphenylHCID 2734937—
Edukt5,5-Dimethylpyrrolidine-2,4-dioneHCID 13346709—
Edukt1-Bromo-5-(4-chlorophenyl)-2-methylbenzeneHCID 59445930—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-[3-(4-Chlorophenyl)-6-methylphenyl]-5,5-dimethylpyrrolidine-2,4-dioneHCID 70496342—

Reaktionsschritte

Under argon, in a heat-dried apparatus, 7.4 mg of Pd(OAc)2, 22 mg of di-tert-butyl(2′-methylbiphenyl-2-yl)phosphine and 0.78 g of K3PO4 in 4.8 ml of air-free dioxane are introduced as initial charge. 203 mg of 5,5-dimethylpyrrolidine-2,4-dione and 659 mg of 3-(4-chlorophenyl)-6-methylbromobenzene are added and the mixture is stirred for 16 hours under reflux. The mixture is then left to cool to room temperature, diluted with ca. 6 ml of methanol and filtered, and the filter residue is after-washed with ca. 3 ml of MeOH. The combined filtrates are concentrated by evaporation on a rotary evaporator. The residue is taken up in ca. 6 ml of water and rendered weakly acidic using 1 N hydrochloric acid. The precipitated solid is filtered off with suction and washed with ca. 3 ml of water. It is then washed from the filter with acetone and the filtrate is concentrated by evaporation. This gives 0.597 g of solid. Reversed-phase separation with water/acetonitrile (gradient) gives 93 mg (14% of theory) with a purity of 98.6% according to HPLC/MS.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859782B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-19eef06fda31456e80a92bd9fadcde1c
Quellennotizuspto-grants-2014_10