HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → Acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Isobutyl ketone | HCID 7958 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | 3,3,5-Trimethylcyclohexanone | HCID 13398 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl ketone | HCID 7288 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | Acetaldehyde | HCID 177 | — |
| Product | Benzaldehyde | HCID 240 | — |
| Product | Butanal | HCID 261 | — |
| Product | Isobutyraldehyde | HCID 6561 | — |
Reaction Steps
Optionally, the polyaminoamide-polyaminoimidazoline mixtures described above, which are to be used according to the present invention, can be reacted with common ketones such as acetone, methyl-ethyl ketone, di-ethyl ketone, methyl-isobutyl ketone, cyclohexanone, cyclopentanone, di-isobutyl ketone, 3,3,5-trimethyl cyclohexanone, or methyl-phenyl ketone, or with aldehydes such as acetaldehyde, butyraldehyde, isobutyraldehyde, or benzaldehyde to form the corresponding Schiff bases or enamines.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146520 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-d86be34e8b3e4a9587888377e234ae88 |
| Source note | uspto-grants-1979_03 |