HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Hexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butyric Acid | HCID 264 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Product | 3-Hexanone | HCID 11509 | 60% |
| Product | Octan-4-one | HCID 11516 | 24% |
Reaction Steps
Kirk-Othmer i.b.i.d. discloses that unsymmetrical dialkyl ketones are prepared by passing vapors of two different fatty acids over an alkaline earth oxide at elevated temperatures. It is stated that the product necessarily contains the three possible ketones and in the example given a mixture of acetic acid and butyric acid are reacted in the vapor phase at 300° C. on a manganese dioxide catalyst to produce 16% methyl ethyl ketone, 24% propyl butyl ketone and 60% ethyl propyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05001273 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-6b7a825e77f247169c607f37de29cc58 |
| Source note | uspto-grants-1991_03 |