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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,2-DimethoxyethaneHCID 8071—
Product8-Benzyl-8-azabicyclo[3.2.1]octane-3-carbonitrileHCID 2213570041.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391883B1
Source datasetuspto-grants-2002_05
ORD IDord-12f113a07ca046d2a6d49430a5e3ac1f
Source noteuspto-grants-2002_05