HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1608794Erstellt: 25. Oktober 2026
Dimethyl Sulfoxide → 2-Benzyl-2-azabicyclo[2.2.2]octane-3,6-dione
https://huagongshe.com/reaction/1608794
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 2-Benzyl-2-azabicyclo[2.2.2]octan-3-one | HCID 13265545 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Benzyl-2-azabicyclo[2.2.2]octane-3,6-dione | HCID 20085697 | 92% |
Reaktionsschritte
A solution of dimethyl sulphoxide (2.34 g) in dichloromethane (5 ml) was added to a cooled (-60° C.) solution of oxalyl chloride (1.78 g) in dichloromethane (5 ml) and after 2 minutes the mixture was treated with a solution of 2-benzyl-2-azabicyclo[2.2.2]octan-3-one (2.31 g--commercially available) in dichloromethane (10 ml), stirred at -60° C. for 30 minutes, treated with triethylamine (5.05 g), allowed to warm up to room temperature, quenched with water and extracted into dichloromethane. The dichloromethane extracts were dried over sodium sulphate and evaporated. The residue was purified by chromatography on silica using hexane plus 50% ethyl acetate as eluant. Appropriate fractions were combined and evaporated to give the desired compound (2.10 g, 92%) as a colourless oil which was used directly in Preparation 3 without characterisation or further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05397800 |
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| Quelldatensatz | uspto-grants-1995_03 |
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| ORD ID | ord-229e77b4d28c4549919d4e8d8f4e776e |
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| Quellennotiz | uspto-grants-1995_03 |
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