HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936725Generated: October 27, 2026
Ethanol → 8-Benzyl-8-azabicyclo[3.2.1]octane-3-carbonitrile
https://huagongshe.com/reaction/1936725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 8-Benzyl-8-azabicyclo(3.2.1)octan-3-one | HCID 119846 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 8-Benzyl-8-azabicyclo[3.2.1]octane-3-carbonitrile | HCID 22135700 | 41.4% |
Reaction Steps
Potassium t-butoxide (2.5 g) was added portion wise to a stirred mixture of 8-benzyl-8-azabicyclo[3.2.1]octan-3-one (2.0 g), tosylmethyl isocyanide (2.36 g) and ethanol (2 ml) in dimethoxyethane (50 ml) at 0° C. under nitrogen. The mixture was stirred at 0° C. for 0.5 hours and then overnight at room temperature. The mixture was then filtered and the solid residue washed with dimethoxyethane. The combined filtrates were evaporated under reduced pressure and chromatographed [SiO2; hexane:ethyl acetate (80:20)] to give 3-cyano-8-benzyl-8-azabicyclo[3.2.1]octane (0.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391883B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-12f113a07ca046d2a6d49430a5e3ac1f |
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| Source note | uspto-grants-2002_05 |
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