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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050899Generated: October 25, 2026

Acetaldehyde → 1-Cyano-1-(4-diethylaminophenyl)cyclopentane

https://huagongshe.com/reaction/2050899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantEthanolHCID 702—
Reactant1-(4-Nitrophenyl)cyclopentane-1-carbonitrileHCID 4351905—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product1-Cyano-1-(4-diethylaminophenyl)cyclopentaneHCID 19834117—

Reaction Steps

In a pressure reactor was placed 43.4 g (0.2 mole) of 1-cyano-1-(4-nitrophenyl)cyclopentane and 500 mL of absolute ethanol. One gram of 5% Pd/C was added, the reactor charged with hydrogen and shaken at room temperature until the theoretical amount of hydrogen had been taken up. The reactor was vented and 22 g (0.5 mole) of acetaldehyde and 2 g of 10% Pd/C was added. The reactor was charged with hydrogen and shaken at room temperature for 16 hours. The reaction mixture was then filtered and the filtrate concentrated in vacuo. The product was purified by chromatography, using a gradient of 90% hexane: 10% ethylacetate to 70% hexane: 30% ethylacetate as eluant. There was obtained 10.7 g of a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015644
Source datasetuspto-grants-1991_05
ORD IDord-0ad487086dea4a00aeb59f61f85a9439
Source noteuspto-grants-1991_05