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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221848Erstellt: 25. Oktober 2026

Sulfuric Acid → 1-(4-Methoxyphenyl)butane-1,3-dione

https://huagongshe.com/reaction/221848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukt4'-MethoxyacetophenoneHCID 7476—
EduktEthyl AcetateHCID 8857—
EduktSodium hydrideHCID 24758—
KatalysatorEthanolHCID 702—
Katalysator18-Crown-6HCID 28557—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Methoxyphenyl)butane-1,3-dioneHCID 7764060,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To 9.80 mL of ethyl acetate (100 mmol) in 40 mL dry THF at room temperature was added 2.0 g of 60% sodium hydride (49.9 mmol), 7.50 g of 4′-methoxyacetophenone (49.9 mmol), 100.0 mg of 18-crown-6 (0.40 mmol), and 2 drops of ethanol. After 30 minutes, the reaction was refluxed for 1 h, and then 100 mL of dry THF was added. After an additional 1 h, 30 mL THF was added. After 1 h the reaction was cooled to 0° C. and 25 mL of 10% aqueous sulfuric acid was added. The product was extracted with diethyl ether. The ether extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 4:1 hexane:ethyl acetate to give 5.8 g of 1-(4-methoxyphenyl)butane-1,3-dione containing 30% starting material (via 1H NMR 42% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207168B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-8c7ebcd2583645af97db7647fa4bff5c
Quellennotizuspto-grants-2012_06