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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582027Generated: October 27, 2026

Ethanol → 8-Benzyl-8-azabicyclo[3.2.1]octane-3-carbonitrile

https://huagongshe.com/reaction/582027

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 portionwise 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 ternperature. 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 numberUS05922732
Source datasetuspto-grants-1999_07
ORD IDord-58ce3e44e6534b2581787e6dac5ed864
Source noteuspto-grants-1999_07