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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1929574Erstellt: 25. Oktober 2026

Citric Acid → 2-Ethoxycarbonyl-3-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-4-methyl-pentanedioic acid 1-tert-butyl ester 5-ethyl ester

https://huagongshe.com/reaction/1929574

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
Edukttert-Butyl ethyl malonateHCID 96345—
EduktHCID 11481404HCID 11481404—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-Ethoxycarbonyl-3-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-4-methyl-pentanedioic acid 1-tert-butyl ester 5-ethyl esterHCID 59326554—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Malonic acid tert-butyl ester ethyl ester (30.08 g, 151.8 mmol) was added to a solution of potassium tert-butoxide (16.30 g, 138.0 mmol) in 200 mL of N,N-dimethyl acetamide, while the reaction temperature was maintained at ˜25° C. To the resulting mixture was then added the solution of 4-(4-fluoro-phenyl)-2-methyl-buta-2,3-dienoic acid ethyl ester prepared above, at such a rate that the reaction temperature was maintained between 20-28° C. After the addition was complete, the reaction mixture was stirred at room temperature for 20 minutes, when HPLC indicated completed reaction. The mixture was then treated with 100 mL of 1M citric acid and 150 mL of ice-water, and then extracted with 400 mL of methyl tert-butyl ether. The organic extract was separated and washed with 2×200 mL of water, and then concentrated to produce 56.36 g of a yellow oil, which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08188090B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-798595b51513453f9a71259e0b5833ab
Quellennotizuspto-grants-2012_05