HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Toluenesulfonyl chloride → HCID 54383240, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Methyl tricyclo(3.3.1.13,7)dec-1-yl ketone | HCID 123126 | — |
| Edukt | (S)-(-)-alpha-Methyl-4-pyridinemethanol | HCID 10920507 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | HCID 54383240 | HCID 54383240 | 18% |
Reaktionsschritte
The method followed that described in Example 9 but using (-)-(S)-1-(4-pyridyl)ethanol (1.84 g, 15.0 mmol) in THF (80 ml), butyllithium (1.6M; 9.4 ml, 15.0 mmol) in hexane, p-toluenesulfonyl chloride (2.86 g, 15.0 mmol), diisopropylamine (6.31 ml, 45.0 mmol) in THF (120 ml), butyllithium (1.6M; 28.12 ml, 45.0 mmol) in hexane and 1-adamantyl methyl ketone (8.0 g, 45 mmol). Chromatography, on elution with petrol-ether-triethylamine 100:50:1 gave the title compound (765 mg, 18%), which crystallised from hexane. m.p. 46°-48° C.; [α]D +6.8° (c 1.0, MeOH). IR, NMR and MS data were the same as given in Example 14.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05595995 |
| Quelldatensatz | uspto-grants-1997_01 |
| ORD ID | ord-7de453a8f75a4c46966a5aafdd216cf3 |
| Quellennotiz | uspto-grants-1997_01 |