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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655097Generated: October 27, 2026

Acetone → 6,10-Dimethylundecan-2-one

https://huagongshe.com/reaction/1655097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant3,7-Dimethylocta-2,6-DienalHCID 8843—
Reactant(3E,5E)-6,10-dimethyl-2-undeca-3,5,9-trienoneHCID 78954—
Reactant3E,5E-PseudoiononeHCID 1757003—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product6,10-Dimethylundecan-2-oneHCID 9549587%

Reaction Steps

A mixture of 17.82 g (92.8 mmoles) of 6,10-dimethyl-3,5,9-undecatrien-2-one ("pseudoionone", prepared from citral and acetone as described by A. Russell, et al., Organic Syntheses, Collective Volume-3, pages 747-750) and 1.0 g of 5% palladium on activated carbon in 50 mL of absolute ethyl alcohol was shaken vigorously under a hydrogen atmosphere (approximately 2-3 atm. pressure) for 30 minutes. After removal of the catalyst by filtration through a small pad of Hyflo Super-Cel® filtering aid, the filtrate was diluted with 150 mL of hexane. The organic layer was subsequently washed with water (2×400 mL), then dried over anhydrous magnesium sulfate, and re-filtered. Removal of the hexane by evaporation at reduced pressure, followed by distillation, afforded 15.95 g (87% yield) of 6,10-dimethyl-2-undecanone: boiling point 68°-72° C. at 0.15 mm. A previous synthesis of the latter ketone has been reported by F. G. Fischer, et al., Ann., 475, 183 (1929).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410094
Source datasetuspto-grants-1995_04
ORD IDord-193e97be710d4574963e646131db0f03
Source noteuspto-grants-1995_04