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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228884Generated: October 31, 2026

Acetone → 6-Methyl-2-heptanone

https://huagongshe.com/reaction/2228884

Reaction equation

Participants

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

Reaction Steps

This latter embodiment is described below in an example of reacting acetone with isovaleraldehyde to produce 6-methylheptan-2-one. The reaction proceeds in situ via the aldolization stage yielding the corresponding β-hydroxyketone, which is not isolated. Under the reaction conditions elimination of water takes place with the formation of 6-methylhept-3-en-2-one, which is selectively hydrogenated by the homogeneously distributed hydrogenation catalyst in the lipophobic alcohol phase to form the corresponding methyl ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417406B1
Source datasetuspto-grants-2002_07
ORD IDord-02b833170e1b42db9865b4bd8b6bfd2e
Source noteuspto-grants-2002_07