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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8598Erstellt: 23. Oktober 2026

Ethyl Acetate → 2-(3,4-Dimethyl-phenyl)-malonic acid dimethyl ester

https://huagongshe.com/de/reaction/8598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt4-Bromo-o-xyleneHCID 68504—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-(Di-tert-butylphosphino)biphenylHCID 2734215—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3,4-Dimethyl-phenyl)-malonic acid dimethyl esterHCID 68897800—

Reaktionsschritte

(In analogy to a procedure given in J. Am. Chem. Soc. 122 (2000), 1360-1370.) To a suspension of Pd(OAc)2 (455 mg), 2-(di-tert.-butylphosphino)-biphenyl (1.21 g) and K3PO4 (39.6 g) in THF (200 ml) dimethylmalonate (12.85 g) and 1-bromo-3,4-dimethyl-benzene 15.0 g) was added under argon. The mixture was refluxed for 16 h, cooled to rt and diluted with EA (300 ml) and filtered. The filtrate was evaporated and the resulting brown oil was purified on silica gel eluting with heptane:EA 4:1 to 1:1 to give 2-(3,4-dimethyl-phenyl)-malonic acid dimethyl ester (16.2 g) as a colourless oil which slowly crystallises. 1H-NMR (300 MHz, CDCl3): 2.25(s, 3H), 2.26(s, 3H), 3.75(s, 6H), 4.59(s, 1H), 7.10–7.20(m, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091201B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a49db3e4ff1840bf80f49c0406a40f8c
Quellennotizuspto-grants-2006_08