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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975630Generated: November 4, 2026

3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl- → 2,2,3-Trimethylcyclopentaneacetaldehyde

https://huagongshe.com/reaction/1975630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-HCID 98497—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product2,2,3-TrimethylcyclopentaneacetaldehydeHCID 2241425590.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A three liter autoclave with a stirrer is charged with 830 g of campholenic aldehyde and 56 g of catalyst Pd(5%)/C. Hydrogen is introduced until the pressure reaches 30 bars. The mixture is heated up to 80° C. with stirring for five hours. The calculated amount of hydrogen is now absorbed. The catalyst is separated by filtration and washed with ethanol. The solvent is removed by vacuum evaporation and 815 g of crude saturated aldehyde are obtained (purity: 95%, GC). The vacuum distillation of the crude through a Widmer column gives 763 g of pure product (purity 95%); bp20 85° C.; nD20 : 1,4553;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288701
Source datasetuspto-grants-1994_02
ORD IDord-09c1fcba6c654e019dc94b973e7802a6
Source noteuspto-grants-1994_02