HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → HCID 17929730, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Hexylamine | HCID 8102 | — |
| Edukt | 1H,3H-Naphtho(1,8-cd)pyran-1,3-dione, 6-bromo- | HCID 66493 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | HCID 17929730 | HCID 17929730 | 74,3% |
Reaktionsschritte
A mixture of 4-bromo-1,8-naphthalic anhydride (21.40 g, 77.2 mmol), n-hexylamine (13.1 mL, 100 mmol), toluene (200 mL), and chloroform (200 mL) was heated to boil for 1 hour. Precipitate formed making stirring difficult. The mixture was acidified with acetic acid, and heating was continued at 90° C. with distillation of chloroform. After all precipitate dissolved, the reaction mixture was poured onto crushed ice (300 g) and acidified with concentrated HCl to pH 1. After the ice melted, the solid was filtered off and dried. The crude product was purified by column chromatography (silica gel, hexane/ethyl acetate 2:1) to give 6-bromo-2-hexyl-1H-benzo[de]isoquinoline-1,3(2H)-dione (20.66 g, 74%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09382424B2 |
| Quelldatensatz | uspto-grants-2016_07 |
| ORD ID | ord-cb714efa8ddb440cbca5d203951d57bd |
| Quellennotiz | uspto-grants-2016_07 |