HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenol → 1H-1,4,7-Triazonine, octahydro-1-[(4-methylphenyl)sulfonyl]-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | 1H-1,4,7-Triazonine, octahydro-1,4,7-tris((4-methylphenyl)sulfonyl)- | HCID 564157 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Hydrogen Bromide | HCID 260 | — |
| Produkt | 1H-1,4,7-Triazonine, octahydro-1-[(4-methylphenyl)sulfonyl]- | HCID 5246952 | 88% |
Reaktionsbedingungen
| Temperatur | 90 °C |
|---|
Reaktionsschritte
1,4,7-Tris(p-toluenesulfonyl)-1,4,7-triazacyclononane (17.56 g, 29.7 mmol) and phenol (21 g, 223.0 mmol) are dissolved in 240 ml of a solution of HBr (33%) in glacial acetic acid. The solution is heated at 90° C. for 30 h. A solid appears after 3 h. After returning to ambient temperature, the mixture is filtered and the solid is washed with diethyl ether (2×80 ml). The hydrobromide salt is dissolved in a 1M sodium hydroxide solution until the pH is of the order of 12 units. The aqueous solution is extracted with chloroform (8×50 ml). The combined organic phases are dried over Na2SO4 and the solvent is evaporated under vacuum. Finally, a white solid is obtained (7.36 g, yield 88%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08945514B2 |
| Quelldatensatz | uspto-grants-2015_02 |
| ORD ID | ord-2caf0f77d101431bafcd0a432140584f |
| Quellennotiz | uspto-grants-2015_02 |