HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,8-Diaminonaphthalene → 2,3-Dihydroperimidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,8-Diaminonaphthalene | HCID 68067 | — |
| Edukt | 4-Chlorobutyrophenone | HCID 253533 | — |
| Katalysator | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2,3-Dihydroperimidine | HCID 12440965 | 47,4% |
Reaktionsschritte
A stirred mixture of 1.411 g of 1,8-diaminonaphthalene, 1.629 g of 4-chlorobutyro-phenone, 3 mg of p-toluenesulfonic acid monohydrate, and 10 mL of toluene was heated to reflux under a nitrogen atmosphere using a Dean-Stark trap to remove the water evolved from the reaction for 10 hr. The mixture was filtered to remove unreacted starting material, partioned between ethyl acetate and 5% sodium hydroxide solution, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give 2.04 g of crude product. This was further purified by chromatography on silica gel, eluting with 1:1 diethyl ether/petroleum ether, and collecting the initial band to yield 0.719 g of dihydroperimidine intermediate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05380635 |
| Quelldatensatz | uspto-grants-1995_01 |
| ORD ID | ord-0afe8927cbfd4921aeee83560246b418 |
| Quellennotiz | uspto-grants-1995_01 |