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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286141Generated: October 31, 2026

2-Cyclohexen-1-one, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)- → Cyclohexanone, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)-

https://huagongshe.com/reaction/2286141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclohexen-1-one, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)-HCID 93696—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventPotassium HydroxideHCID 14797—
ProductCyclohexanone, 3,5-dimethyl-4-(3-methyl-2-buten-1-yl)-HCID 2046926387.4%

Reaction Steps

A solution of 3,5-dimethyl-4-(3-methyl-2-butenyl)-2-cyclohexen-1-one (8.2 g, 0.043 mol) in 0.3 M ethanolic KOH (16 mL) was hydrogenated at room temperature and 1 atmosphere over 5% palladium on carbon (0.8 g). After uptake of 1 equivalent of hydrogen, the solution was filtered through Celite and concentrated. The residue was partitioned between hexane and water; then the hexane layer was dried (Na2SO4) and the solvent removed on a rotary evaporator. Kugelrohr distillation gave 7.3 g of 3,5-dimethyl-4-(3-methyl-2-butenyl) cyclohexanone, bp 115° C./0.5 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04326996
Source datasetuspto-grants-1982_04
ORD IDord-90c556e4443d4828b49119ceb5ec21c7
Source noteuspto-grants-1982_04