Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278098Erstellt: 25. Oktober 2026

1-(Triphenylphosphoranylidene)acetone → Methyl 3-(3-oxo-1-butenyl)indole-6-carboxylate

https://huagongshe.com/reaction/278098

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Eduktmethyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktMethyl 3-(3-oxo-1-butenyl)indole-6-carboxylateHCID 5385828217%

Reaktionsschritte

To a stirred solution of methyl 3-formylindole-6-carboxylate (368 mg) in 1,4-dioxane (10 ml) was added acetylmethylene triphenylphosphorane (1.15 g), and the mixture was stirred under reflux for 12 hours. The resulting mixture was evaporated in vacuo, redissolved with ethyl acetate and washed with 1N hydrochloric acid and brine. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a mixture of chloroform and ethyl acetate (1:2) to give methyl 3-(3-oxo-1-butenyl)indole-6-carboxylate (75 mg) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358992B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e5b7b3b9a0b94d1a9039241ad2e1a667
Quellennotizuspto-grants-2002_03