HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (E)-1,1-Dimethoxy-6,10-dimethyl-5,9-undecadien-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Geraniol | HCID 637566 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2E)- | HCID 5365867 | — |
| Reactant | Methyl 4,4-dimethoxy-3-oxobutanoate | HCID 11008445 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-1,1-Dimethoxy-6,10-dimethyl-5,9-undecadien-2-one | HCID 11139695 | — |
Reaction Steps
In 350 ml of anhydrous ethanol was dissolved 17.4 g of sodium metal, and to this was added dropwise 160 g of methyl 4,4-dimethoxyacetoacetate with stirring at room temperature. One hour later, geranyl bromide prepared from 130 g of geraniol was added dropwise to the above-obtained mixture under ice-cooling. The mixture was then allowed to stand overnight at room temperature and refluxed for one hour. To this reaction mixture was added 42 g of sodium hydroxide in a mixture of 1.4 1. of ethanol and 1.18 1. of water, and the mixture was heated under reflux for 6 hours and extracted with n-hexane. The n-hexane extract was distilled under reduced pressure to give 134 g of the desired product, b.p. 92°-95° C./0.05 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260551 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-227598ca0b104909abaeec2811c0581d |
| Source note | uspto-grants-1981_04 |