HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68535Erstellt: 25. Oktober 2026
Toluene → 4-(2-Fluoro-4-nitrophenyloxy)-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinoline
https://huagongshe.com/reaction/68535
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 2-Fluoro-4-nitrophenol | HCID 9825 | — |
| Edukt | 4-Chloro-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinoline | HCID 22646630 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(2-Fluoro-4-nitrophenyloxy)-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinoline | HCID 86696917 | 285,5% |
Reaktionsschritte
2-fluoro-4-nitrophenol (36.73 g, 0.234 mol) was added to a dried chlorobenzene (5v/w, 250 mL). The mixture was heated to 145° C. Intermediate VII (12.5 g, 0.039 mol) was added to the reaction solution. The reaction was conducted at this temperature for 20 h. After completion of the reaction, the solvent was evaporated off to produce a grey solid. This solid was dissolved in CH2Cl2, and washed with a satureated saturated K2CO3 solution several times. The organic layer was collected. The solvent was dried off to produce a solid, which is recrystallized with ethanol to produce a yellow solid (49.16 g) in a yield of 71.4%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08822465B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-f066b89403a94d5eaa5d9770d18a2c39 |
|---|
| Quellennotiz | uspto-grants-2014_09 |
|---|