HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1,3-Diiodopropane | HCID 12314 | — |
| Edukt | 1,4,7-Triazacyclononane | HCID 188318 | — |
| Edukt | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| Produkt | HCID 17939386 | HCID 17939386 | — |
Reaktionsschritte
N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-Bis[N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluenesulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06387891B2 |
| Quelldatensatz | uspto-grants-2002_05 |
| ORD ID | ord-b718a5cbb0b444359a2bff50bdcc59e6 |
| Quellennotiz | uspto-grants-2002_05 |