Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 1,7-Octadiyne | HCID 70099 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Deca-2,8-diyne-1,10-diol | HCID 14168564 | 50% |
Reaktionsschritte
2.12 g of commercially available 1,7 octadiyne (20.0 mmol) was first combined with 80 mL of Et2O and 30 mL of THF. The solution was cooled to -78° C. and treated with 15.6 mL (42 mmol, 2.7M) of BuLi. After 0.5 hr at this temperature, 4.8 g of paraformaldehyde (160 mmol) was added and stirred for a further 2.0 hr at 0° C. At 10% soln. of aqueous HCl was added and the crude product extracted into diethyl ether. Treatment of the ether extracts with sat. NaHCO3 and brine, followed by solvent removal and column chromatography (60:40 EtOAc: Hexane) gave pure deca-2,8-diyne-1,10-diol in 50% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05436361 |
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| Quelldatensatz | uspto-grants-1995_07 |
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| ORD ID | ord-b19e511fb21e461cbc8699424a744fa4 |
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| Quellennotiz | uspto-grants-1995_07 |
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