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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-QuinuclidinoneHCID 19507—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-Azabicyclo(2.2.2)octane-3-carbonitrileHCID 14286574%

Reaction Conditions

Temperature4 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968691
Source datasetuspto-grants-1990_11
ORD IDord-961b427036834866a204bcc7a2be52ce
Source noteuspto-grants-1990_11