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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4950Generated: October 23, 2026

Acetic Acid → HCID 10492977, compound

https://huagongshe.com/en/reaction/4950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN1-(3-chlorophenyl)ethane-1,2-diamineHCID 11008376—
SolventMethanolHCID 887—
ProductHCID 10492977HCID 104929773.7%

Reaction Steps

To a stirred solution of N-(3-chlorophenyl)-1,2-diaminoethane (1 g; 0,00586 moles) in 25 ml of anhydrous methanol kept under nitrogen atmosphere, 3-quinuclidinone hydrochloride (1.01 g, 0.0062? moles) is added. The pH is adjusted to pH 6 by addition of glacial acetic acid. Sodium cyanoborohydride (0.74 g; 0.0117 moles) is added in two portions. The reaction mixture is refluxed for 10 hours, cooled and then filtered. After evaporation to dryness the residue is taken up with water, basified with 20% sodium hydroxide solution and extracted three times with ethyl acetate. The organic layer is washed with brine, dried over anhydrous sodium sulfate and, after filtration, evaporated to dryness. The residue is purified by silica gel flash-chromatography (methylene chloride--methanol--30% ammonium hydroxide, 150:50:5 as eluant) to give the desired product as a clear oil (0.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242929
Source datasetuspto-grants-1993_09
ORD IDord-6155d4e4a76d41d69a88452893850b2d
Source noteuspto-grants-1993_09