HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 588335Erstellt: 24. Oktober 2026
1,2-Dimethoxyethane → 1-Azabicyclo(2.2.2)octane-3-carbonitrile
https://huagongshe.com/de/reaction/588335
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | 3-Quinuclidinone | HCID 19507 | — |
| Edukt | Tosylmethyl isocyanide | HCID 161915 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-Azabicyclo(2.2.2)octane-3-carbonitrile | HCID 142865 | — |
Reaktionsschritte
20.4 g (163 mmol) of 3-quinuclidinone and 41.4 g (212 mmol) of (4-toluenesulfonyl)methyl isocyanide are introduced into 435 ml of 1,2-dimethoxyethane and 16 ml of dry ethanol while cooling in ice. 45.7 g (407 mmol) of potassium tert-butoxide are slowly added in such a way that the temperature does not rise above 10° C. The mixture is then heated at 40° C. for 2.5 h. After cooling to RT, the resulting solid is filtered off. The filtrate is concentrated and chromatographed on neutral alumina (mobile phase: dichloromethane→ethyl acetate→ethyl acetate/methanol 50:1). 22.9 g (quant.) of the racemic product are obtained in slightly impure form.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09227964B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-0c15cf9fcccf45428de45158e4dc2c28 |
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| Quellennotiz | uspto-grants-2016_01 |
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