HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918314Generated: October 31, 2026
Ethanol → trans Ethyl 11-ethoxy-3,7,11-trimethyldodeca-2,4-dienoate
https://huagongshe.com/reaction/918314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | trans Ethyl 3,7,11-trimethyldodeca-2,4,10-trienoate | HCID 86733725 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans Ethyl 11-ethoxy-3,7,11-trimethyldodeca-2,4-dienoate | HCID 86733726 | — |
Reaction Steps
Fifteen grams of mercuric acetate in 50 ml. of dry ethanol is added to 12 g. of trans ethyl 3,7,11-trimethyldodeca-2,4,10-trienoate in 30 ml. of dry ethanol cooled in an ice bath. The temperature is allowed to come to room temperature by standing overnight. Then the mixture is cooled to 0°, 10 g. of potassium hydroxide in 150 ml. of ethanol is added followed by addition of 1.0 g. of sodium borohydride in small portions. After about 30 minutes at 0°, water is added and mixture left at room temperature for 2 hours. The mixture is filtered, filtrate concentrated and extracted with ether. The ethereal extract is washed, dried, and evaporated to yield trans ethyl 11-ethoxy-3,7,11-trimethyldodeca-2,4-dienoate which is purified by distillation or chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03970704 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-2a1451b7b3984e92b3a7b30d87edd834 |
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| Source note | uspto-grants-1976_07 |
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