HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 6-Methyl-2-heptanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 3-Methylbutanal | HCID 11552 | — |
| Product | 6-Methyl-2-heptanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06417406B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-02b833170e1b42db9865b4bd8b6bfd2e |
| Source note | uspto-grants-2002_07 |