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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828634Generated: October 30, 2026

Sodium Cyanide → 2-{1-Azabicyclo[2.2.2]octan-4-yl}acetonitrile

https://huagongshe.com/reaction/1828634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethanesulfonateHCID 85257—
Reactant1-Azabicyclo(2.2.2)octane-4-methanolHCID 141311—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product2-{1-Azabicyclo[2.2.2]octan-4-yl}acetonitrileHCID 2205663572%

Reaction Steps

Quinuclidin-4-ylmethanol (1.94 g, 0.014 moles) was converted to the corresponding mesylate by treatment with methane sulphonyl chloride and triethylamine in chloroform. The mesylate was dissolved in dimethylformamide (50 ml) and treated with sodium cyanide (1.4 g, 0.028 moles) at 120° C. for 18 hours. The mixture was cooled and concentrated in vacuo. The residue was partitioned between saturated potassium carbonate and chloroform. The organic layer was separated and dried (Na2SO4), filtered and evaporated to dryness. Chromatography on silica gel eluting with 0-10% methanol/chloroform gave the title compound 1.5 g (72%). M.S. (+ve electrospray) m/z 151 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039128E1
Source datasetuspto-grants-2006_06
ORD IDord-8dc3a37869ce47f2873cb89613cbee46
Source noteuspto-grants-2006_06