Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | Butyryl chloride | HCID 8855 | — |
| Edukt | 1,2-Diethenylbenzene | HCID 66666 | — |
| Katalysator | Aluminum(III) Chloride | HCID 6451240 | — |
| Produkt | Butyrophenone | HCID 10315 | — |
Reaktionsschritte
About 50 grams of resin beads of polystyrene that has been copolymerized with about 1% divinylbenzene are stirred at room temperature for about 2 hours in butyryl chloride with aluminum chloride as a catalyst, namely Friedel-Crafts conditions. Reaction occurs with the benzene moieties on the resin to form butyrophenone or propylphenylketone. These resulting ketone moieties are then subjected to the Leukardt-Wallach reduction amination reaction using N-propyl formamide to produce N-propyl α-aminobenzyl moieties. The step-by-step synthesis of the nonapeptide as set forth in Example I is repeated. Cleavage, deprotection and purification are carried out under the same conditions and are found to produce the nonapeptide amide having the following formula:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04701499 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-391515ef7ed54614934d87ce74b4052c |
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| Quellennotiz | uspto-grants-1987_10 |
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