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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68292Erstellt: 24. Oktober 2026

Diethyl Oxalate → 4-(2-Methoxyphenyl)-2,4-dioxobutanoic acid

https://huagongshe.com/de/reaction/68292

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt2-Methoxy-1-phenylethanoneHCID 77698—
EduktSodium ethoxideHCID 2723922—
LösungsmittelEthanolHCID 702—
Produkt4-(2-Methoxyphenyl)-2,4-dioxobutanoic acidHCID 510669—

Reaktionsschritte

To a stirred solution of diethyl oxalate (16 g, 110 mmol) and sodium ethoxide (100 mL, 21% by wt. in ethanol, 300 mmol) was added dropwise a solution of 2-methoxy acetophenone (15 g, 100 mmol) in ethanol (100 mL). The reaction mixture was allowed to stir at ambient temperature overnight. The resulting solution was concentrated to approximately 50 mL on a rotary evaporator, followed by partitioning between diethyl ether (100 mL) and water (250 mL). The aqueous layer was adjusted to pH=3 with conc. HCl to give a suspension with a fine white precipitate, which was heated at 100° C. for 5-10 minutes followed by cooling in an ice bath for 1 h. The precipitate was filtered, washed with water (20 mL), and dried overnight under high vacuum to give 4-(2-methoxyphenyl)-2,4-dioxobutanoic acid. 1H NMR (300 MHz, CDCl3) δ 7.96 (q, J=9.0, 3.0 Hz, 1H), 7.53 (t, J=6.0 Hz, 1H), 7.47 (s, 0.9H keto form), 7.24 (s, 1.1H enol form), 7.06 (t, J=6.0 Hz, 1H), 7.00 (d, J=9.0 Hz, 1H), 3.97 (s, 3H). ESI-MS m/z 220.9 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822451B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-138099f9b9bc4db68d4847dda14acc01
Quellennotizuspto-grants-2014_09