HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 2-(2,4-Dinitrophenoxy)-1H-isoindole-1,3(2H)-dione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | 1-Bromo-2,4-dinitrobenzene | HCID 11441 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-(2,4-Dinitrophenoxy)-1H-isoindole-1,3(2H)-dione | HCID 7036309 | 96,4% |
Reaktionsschritte
To a suspension of 2-hydroxyisoindoline-1,3-dione (20.0 g, 0.12 mol) in acetone (400 mL) was added Et3N (14.9 g, 0.15 mol), the mixture was stirred at room temperature until it became a homogeneous solution, then 1-bromo-2,4-dinitrobenzene Y-1 (30.2 g, 0.12 mol) was added. The reaction was stirred at room temperature for 3 h, then poured into ice-water, the resulting precipitate was filtered and washed three times with cold MeOH, dried in vacuum to afford the title compound (38.1 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08987269B2 |
| Quelldatensatz | uspto-grants-2015_03 |
| ORD ID | ord-dbb3f970c0724ff3a7a479fecd60add1 |
| Quellennotiz | uspto-grants-2015_03 |