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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368175Generated: October 27, 2026

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

https://huagongshe.com/reaction/1368175

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 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 stifled 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 numberUS06573275B1
Source datasetuspto-grants-2003_06
ORD IDord-d3c4e46798e24d3cb16b577a69dbe489
Source noteuspto-grants-2003_06