Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | HCID 13886689 | HCID 13886689 | — |
| Reactant | HCID 178503025 | HCID 178503025 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3E,5E,8Z)-1,3,5,8-Undecatetraene | HCID 5352366 | 20% |
| Product | Finavarrene | HCID 5352368 | 20% |
Reaction Steps
(5Z,8Z)-1,5,8-undecatrien-3-ol (3.0 g, 18.1 mmol), 60 ml of hexamethylphosphoric triamide (HMPTA) and 16.4 g (36.2 mmol) of methyl(triphenoxy)phosphonium iodine (MTPI) were added to a reactor under a nitrogen atmosphere followed by stirring at room temperature for 3 hours and at 50° C. for 1 hour. The reaction was stopped by addition of 50 ml of ice water followed by extracting with pentane. After the organic layer was washed with a saturated aqueous sodium chloride solution, it was dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was subjected to a chromatographic treatment using pentane to give 2.0 g (yield: 74%) of a crude product. The resultant crude product (0.5 g, 3.37 mmol) was further purified by a chromatography using pentane and diethyl ether to give 0.05 g (yield: 20%) of (3E,5Z,8Z)-1,3,5,8-undecatetraene and 0.05 g (yield: 20%) of (3E,5E,8Z)-1,3,5,8-undecatetraene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749551B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-45fda99b4fb8441b8a76d1bb712b702c |
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| Source note | uspto-grants-2010_07 |
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