Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273327Erstellt: 25. Oktober 2026

Bromoacetone → 7-Methoxy-2-methylindolizine

https://huagongshe.com/reaction/273327

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetoneHCID 11715—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt4-Methoxy-2-methylpyridineHCID 4737758—
LösungsmittelBenzeneHCID 241—
Produkt7-Methoxy-2-methylindolizineHCID 5295161831%

Reaktionsschritte

4-Methoxy-2-methylpyridine (0.123 g, 1 mmol) and bromoacetone (0.16 mL, 1 mmol) were heated at 95° C. under N2 for 2 h. 1,8-Diazabicyclo-[5.4.0]-undec-7-ene (0.34 mL, 2.2 mmol) in benzene (10 mL) was added. The mixture was then refluxed under N2 for 1 h, poured into ice water, and then extracted with EtOAc. The combined organic layers were washed with water and dried. After the solvent was removed in vacuo, the residue was purified on a silica gel column eluting with EtOAc:Hexane (1:9) and EtOAc to give 7-methoxy-2-methylindolizine (0.050 g, 31%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456289B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-6df95fb68b7c47248a73d1d03ad07ace
Quellennotizuspto-grants-2008_11