HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 609642Erstellt: 23. Oktober 2026
Phenyl isocyanate → N-Phenylcarbamic Acid (3S)-1-azabicyclo[2.2.2]octan-3-yl Ester
https://huagongshe.com/de/reaction/609642
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phenyl isocyanate | HCID 7672 | — |
| Edukt | 3-Quinuclidinol, (+)- | HCID 736411 | — |
| Katalysator | Di-n-butyldilauryltin | HCID 9809426 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-Phenylcarbamic Acid (3S)-1-azabicyclo[2.2.2]octan-3-yl Ester | HCID 684226 | 90,4% |
Reaktionsschritte
A solution of (3S)-(+)-quinuclidin-3-ol (0.50 g, 3.93 mmol) [M. Langlois, C. Meyer, and J. L. Soulier, Synth. Comm., 23, 1895-1911 (1992)], phenyl isocyanate (0.47 mL, 4.32 mmol, 1.1 equivalents), and dibutyltin dilaurate (0.013 mL, 0.08 mmol) in anhydrous toluene (20 mL) was heated at reflux under nitrogen for 1 hour. The resulting reaction mixture was evaporated under reduced pressure, and the resulting solid was placed in 1N HCl (25 mL). The resulting aqueous mixture was extracted with ethyl acetate (2×25 mL), basified to pH 10 with Na2CO3, and extracted with chloroform (3×50 mL). The chloroform extracts were combined, dried (MgSO4), and evaporated under reduced pressure. The resulting solid was recrystallized using toluene (5 mL) to afford the title compound (0.875 g, 90%) as a white solid: mp 129.0-130.0° C.; FAB LRMS m /z (relative intensity, %) 247 (MH+, 39), 110 (100); [α]22D =-7.5° (c=1.0, MeOH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05998429 |
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| Quelldatensatz | uspto-grants-1999_12 |
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| ORD ID | ord-6e7836553f1d4913a5a5f3c719f7e0c8 |
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| Quellennotiz | uspto-grants-1999_12 |
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