HuagongsheHuagongshe Chemistry Print Report · For research reference only
Mesityl oxide → 2,8-Dimethylnona-2,7-dien-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Mesityl oxide | HCID 8858 | — |
| Reactant | 1-Chloro-3-methyl-2-butene | HCID 10429 | — |
| Reactant | Diacetone Alcohol | HCID 31256 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,8-Dimethylnona-2,7-dien-4-one | HCID 13244984 | — |
Reaction Steps
Acetone under the reaction conditions forms also some diacetone alcohol and mesityl oxide, and these then react with the prenyl chloride to produce the above isomers of prenyl mesityl oxide, also called prenyl-substituted methyl pentenones, in the same manner as acetone reacts with prenyl chloride to produce methyl heptenone. It is also possible that prenyl chloride reacts with the diacetone alcohol in the same manner to give the corresponding hydroxy derivatives that subsequently dehydrate. The presence of such hydroxy ketones is observed in the residues of the methyl heptenone production by the process of U.S. Pat. No. 3,668,255.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04153633 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-5236353093b34b51b46c7a3bb94a86ea |
| Source note | uspto-grants-1979_05 |