Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579467Erstellt: 23. Oktober 2026

Methanol → Ethyl 4-methoxy-3-oxobutanoate

https://huagongshe.com/de/reaction/579467

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt3-Bromo-7-hydroxy-4-methylchromen-2-oneHCID 5337545—
LösungsmittelHydrochloric AcidHCID 313—
ProduktEthyl 4-methoxy-3-oxobutanoateHCID 1264509915,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

NaH (7.71 g, 192.7 mmol) was suspended in DMF (110 mL). The solution of MeOH (2.64 g, 82.5 mmol) in DMF (55 mL) was added drop wise at 0° C. After that, the mixture was stirred at 0° C. for 30 min. The solution of compound 1 (9.54 g, 57.9 mmol) in DMF (55 mL) was added dropwise at 0° C., then the reaction mixture was allowed to warm slowly to RT and stirred for 16 h. The reaction mixture was diluted with 1N HCl (400 mL), extracted with MTBE (250 mL×3). The combined organic layer was washed with H2O (200 mL×5), dried over Na2SO4, filtered, concentrated, purified by silica gel column (PE:EA=10:1) afforded ethyl 4-methoxy-3-oxobutanoate (1.4 g, 15.1%) as light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040714B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-9e7544d2fee74e90bb23995b25649632
Quellennotizuspto-grants-2015_05