Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloride | HCID 312 | — |
| Edukt | Hexamethylphosphoramide | HCID 12679 | — |
| Edukt | 6-Methyl-5-hepten-1-yne | HCID 519983 | — |
| Edukt | Ethyl acetate hexane | HCID 21226206 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Diethylether hexane | HCID 21584099 | — |
| Produkt | (E)-6,10-dimethyl-5,9-undecadien-1-ol | HCID 21631159 | 74% |
Reaktionsschritte
A solution of 198 mL (58.0 mmol) of 0.29M Example 1, Part B-(2) Grignard reagent in THF and 48 mL (275.9 mmol) of HMPA at 0° C. under argon was treated dropwise with 2.0 g (11.6 mmol) of Example 6, Part A chloride in 20 mL of THF. After addition, the reaction was allowed to warm to room temperature for 2 hours, at which point the reaction was diluted with 1:1 hexane/ether and quenched with 1N HCl solution. THe organic layer was washed with 1N HCl followed by water, saturated sodium bicarbonate, brine, dried over MgSO4 and evaporated to provide 3.59 g of crude oil. Flash chromatography was performed on 360 g of silica gel packed and loaded with 10:1 hexane/EtOAc and eluted with 7:1 hexane/ EtOAc collecting 30 mL fractions. Fractions 32 to 49 were combined and evaporated to provide 1.68 g (74%) of title compound in the form of an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428028 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-b9e6498772594cfd863c233c393a8d7d |
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| Quellennotiz | uspto-grants-1995_06 |
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