HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611062Generated: October 25, 2026
Sodium Hydroxide → ethyl(2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate
https://huagongshe.com/reaction/1611062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 15-Crown-5 | HCID 36336 | — |
| Reactant | Citral | HCID 638011 | — |
| Reactant | Triethyl-3-methyl-4-phosphonocrotonate | HCID 86584517 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ethyl(2E,4E,6E)-3,7,11-trimethyl-2,4,6,10-dodecatetraenoate | HCID 6370567 | 876.6% |
Reaction Steps
15-crown-5 (0.9 g, 0.1 equivalents, 4.0 mmol) was dissolved in 50 ml of toluene at room temperature, and added with 32 ml of 50% aqueous sodium hydroxide solution. To the solution, triethyl-3-methyl-4-phosphonocrotonate (11.1 g, 1.05 equivalents, 42 mmol) and then 7 ml toluene solution of geranial (6.1 g, 40 mmol) were added under stirring at 0° C. The mixture was stirred at room temperature for 1.5 hours. The organic and aqueous layers were separated, and the organic layer was washed with saturated ammonium chloride solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 9.2 g of the title compound (yield 87%, 2E:2Z=93:7) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06984742B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-98e6691ebbb24afc9643ea9b2839a1a7 |
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| Source note | uspto-grants-2006_01 |
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