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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370775Generated: October 25, 2026

Acetone → 6-Methyl-2-heptanone

https://huagongshe.com/reaction/1370775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant3-MethylbutanalHCID 11552—
Product6-Methyl-2-heptanoneHCID 13572—

Reaction Steps

To aid comprehension, the reaction will be explained here by the example of the reaction of acetone with isovaleraldehyde to produce 6-methylheptan-2-one. The reaction takes place “in situ” via the stage of aldol condensation with the formation of the corresponding β-hydroxyketone, which is not isolated. Dehydration to 6-methylhept-3-en-2-one takes place under the reaction conditions, and this is hydrogenated selectively to the corresponding methylketone with the hydrogenation catalyst distributed homogeneously in the aqueous catalyst phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583323B2
Source datasetuspto-grants-2003_06
ORD IDord-f282adfabe8d45cda6642831763bf31f
Source noteuspto-grants-2003_06