HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Bromoacetone → 7-Methoxy-2-methylindolizine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Bromoacetone | HCID 11715 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | 4-Methoxy-2-methylpyridine | HCID 4737758 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 7-Methoxy-2-methylindolizine | HCID 52951618 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07456289B2 |
| Quelldatensatz | uspto-grants-2008_11 |
| ORD ID | ord-6df95fb68b7c47248a73d1d03ad07ace |
| Quellennotiz | uspto-grants-2008_11 |