HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 976288Erstellt: 24. Oktober 2026
1,2-Dimethoxyethane → 1-Azabicyclo(2.2.2)octane-3-carbonitrile
https://huagongshe.com/de/reaction/976288
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | 3-Quinuclidinone | HCID 19507 | — |
| Edukt | 1-Isocyanatomethanesulfonyl-4-methylbenzene | HCID 11789078 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-Azabicyclo(2.2.2)octane-3-carbonitrile | HCID 142865 | 74,5% |
Reaktionsschritte
A solution of potassium tert-butoxide (18.27 ml) in 1:1 (v/v) mixture of dimethoxyethane and ethanol (100 ml) was added slowly to a stirred mixture of 3-quinuclidinone (8.14 g), tosylmethylisocyanate (16.53 g) in dry ethanol (6.5 ml), and dry dimethoxyethane (228 ml) under an atmosphere of argon whilst maintaining the temperature below 10° C. The reaction mixture was allowed to warm to ambient temperature and stirred at this temperature for 30 minutes. The reaction mixture was then stirred at 40° C. for 3 hours. The reaction mixture was cooled, filtered and the filtrate evaporated. The residue was purified by flash column chromatography on alumina (Brockmann Grade I) using a 2:98 (v/v) mixture of methanol/ethyl acetate as eluant to give 3-cyanoquinuclidine (6.6 g), microanalysis, found: C, 67.6; H, 8.5; N, 18.7%; C8H12N2 requires: C, 70.6; H, 8.8; N, 20.6%; NMR (CDCl3): 1.4-1.7 (3H, m), 1.85-2.0 (1H, m) 2.0-2.1 (1H, m) and 2.6-3.4 (7H, m); m/z 137 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05612352 |
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| Quelldatensatz | uspto-grants-1997_03 |
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| ORD ID | ord-674cbd93d49343d395987c36d51fabd6 |
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| Quellennotiz | uspto-grants-1997_03 |
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