HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20344597, compound → HCID 20344592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20344597 | HCID 20344597 | — |
| Reactant | HCID 54385261 | HCID 54385261 | — |
| Catalyst | Vanadium | HCID 23990 | — |
| Product | HCID 20344592 | HCID 20344592 | — |
Reaction Steps
2,5,7-Trimethyl-1,4-octadien-3-one can be prepared, for example, from 2,4,7-trimethyl-7-octen-5-yn-4-ol by propargylic rearrangement in a manner known per se with the aid of a vanadium catalyst. By catalytically hydrogenating the resulting dienone at room temperature, as described hereinbefore, there is obtained 2,5,7-trimethyl-3-octanone. 6,8-Dimethyl-3-nonen-2-one can be prepared, for example, by aldol condensation of 3,5-dimethyl-hexanal with acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198532 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-5f2034643aa846f88f01fbe3b22ef08e |
| Source note | uspto-grants-1980_04 |