HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 4-(2-Phthalimidoethyloxy)pyridine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- | HCID 11325 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | HCID 178418642 | HCID 178418642 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(2-Phthalimidoethyloxy)pyridine | HCID 19079211 | 3,1% |
Reaktionsschritte
To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 13.97 g (55 mmol) of N-(2-bromoethyl)phthalimide in 80 ml of DMF, 8.23 ml (55 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added. The mixture was stirred at room temperature for 32 hours. After the solvent was distilled off, the mixture was poured into water and extracted with ethyl acetate. The mixture was washed with water and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 0.41 g of the desired compound (yield: 3.1%, colorless crystal).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05246948 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-73cf2bb5afde4483b79e29dae5dd822c |
| Quellennotiz | uspto-grants-1993_09 |