Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Methoxy-6-methylheptan-2-one | HCID 14631561 | — |
| Reactant | Triphenyl 2,2-ethylenedioxy-pentyl phosphonium bromide | HCID 86734835 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 77886384 | HCID 77886384 | 42% |
Reaction Steps
8.15 g of potassium tert.-butylate were added to a solution of 38 g of triphenyl 2,2-ethylenedioxy-pentyl phosphonium bromide in 400 ml of dimethylformamide cooled to 0° C. and then 12.75 g of 6-methoxy-6-methyl-2-heptanone were added. The mixture was stirred for 4 hours at 0° C. and was then poured into water. The mixture was extracted with petroleum ether (b.p.= 40°-75° C.) and the extracts were washed with water, dried over sodium sulfate and evaporated to dryness. The yellow oil was chromatographed over silica and was eluted with a 8-2 benzene-ethyl acetate mixture to obtain 9.15 g of 2,2-ethylenedioxy-10-methoxy-6,10-dimethyl-5-undecene in the form of a colorless oil which was a mixture of the E and Z isomers with respect to the double bond in the 5-position. A supplementary chromatography under pressure and elution with a 9-1 benzene-ethyl acetate mixture gave a separation of the E and Z isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028386 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-2c1f00dccba246528533833ce4777a26 |
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| Source note | uspto-grants-1977_06 |
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