HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lavandulol, (+-)- → Npc106106
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lavandulol, (+-)- | HCID 94060 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | HCID 87843343 | HCID 87843343 | — |
| Product | Npc106106 | HCID 110898 | — |
Reaction Steps
Tabata has reported the synthesis of 2-isopropylidene-5-methyl-4-hexenyl butyrate in which 2-isopropenyl-5-methyl-4-hexenol as a starting material is subjected to an oxidation reaction with Dess-Martin reagent to form 2-isopropenyl-5-methyl-4-hexenal (lavandulal), the resulting aldehyde is isomerized under an acidic condition through migration of the double bond to form 2-isopropylidene-5-methyl-4-hexenal (another name: fujikonal), and the isomerized aldehyde is reduced and then esterified to form 2-isopropylidene-5-methyl-4-hexenyl butyrate (Appl. Entomol. Zool., 48, 229-232 (2013)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126920B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-18a7de2dc16a4c0a9944eb5c5d29a87f |
| Source note | uspto-grants-2015_09 |