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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013129Generated: October 30, 2026

Water → 2-(Pyridin-3-ylmethylidene)-1-azabicyclo[2.2.2]octan-3-one

https://huagongshe.com/reaction/1013129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
SolventMethanolHCID 887—
Product2-(Pyridin-3-ylmethylidene)-1-azabicyclo[2.2.2]octan-3-oneHCID 61182282%

Reaction Steps

Potassium hydroxide (56 g, 0.54 mole) was dissolved in methanol (420 mL). 3-Quinuclidinone hydrochloride (75 g, 0.49 mole) was added and the mixture was stirred for 30 min at ambient temperature. 3-Pyridinecarboxaldehyde (58 g, 0.54 mole) was added and the mixture stirred for 16 h at ambient temperature. The reaction mixture became yellow during this period, with solids caking on the walls of the flask. The solids were scraped from the walls and the chunks broken up. With rapid stirring, water (390 mL) was added. When the solids dissolved, the mixture was cooled at 4° C. overnight. The crystals were collected by filtration, washed with water, and air dried to obtain 80 g of yellow solid. A second crop (8 g) was obtained by concentration of the filtrate to ˜10% of its former volume and cooling at 4° C. overnight. Both crops were sufficiently pure for further transformation (88 g, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981906B2
Source datasetuspto-grants-2011_07
ORD IDord-79e2de3297b148138ef1d4b64bddecee
Source noteuspto-grants-2011_07