HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetone → 6-Methyl-2-heptanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | 3-Methylbutanal | HCID 11552 | — |
| Produkt | 6-Methyl-2-heptanone | HCID 13572 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06583323B2 |
| Quelldatensatz | uspto-grants-2003_06 |
| ORD ID | ord-f282adfabe8d45cda6642831763bf31f |
| Quellennotiz | uspto-grants-2003_06 |