HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073113Generated: October 28, 2026
Ethanol → 1-Azabicyclo(2.2.2)octane-3-carbonitrile
https://huagongshe.com/reaction/1073113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Quinuclidinone | HCID 19507 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-Azabicyclo(2.2.2)octane-3-carbonitrile | HCID 142865 | 74% |
Reaction Steps
A mixture of 3-quinuclidinone (12.5 g; 0.10 moles), tosylmethyl isocyanide (25.4 g; 0.13 moles) and dry ethanol (10 ml; 0.17 moles) in dry dimethoxyethane (350 ml) was cooled in ice and treated portionwise with potassium t-butoxide (28.0 g; 0.25 moles) while maintaining the temperature between 5° C. and 10° C. After addition was complete the ice bath was removed and stirring was continued for a further 30 min. The reaction was then heated at 4° C. for 2.5 h. After cooling, the precipitate was filtered off and the filtrate concentrated in vacuo. Purification on neutral alumina (Brockmann grade 1) using 2% methanol in ethyl acetate as eluant afforded the title compound as a syrup (10.0 g: 74%) which crystallised on cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968691 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-961b427036834866a204bcc7a2be52ce |
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| Source note | uspto-grants-1990_11 |
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