Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 3-Methyl-1-pentanol | HCID 11508 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Hypobromous acid | HCID 83547 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 8-(3-Methylpentyloxy)octanol | HCID 22407999 | — |
Reaktionsschritte
To a solution of 1.67 gms of 3-methyl pentanol in 40 ml of dimethylformamide, 0.62 gms of sodium hydride are added; and the reaction mixture is stirred at room temperature for 1 hour. To this solution is added 4.0 gms of the protected bromo-alcohol and the reaction mixture is stirred at room temperature for 17 hours. The reaction mixture is then partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give a yellow liquid. To a solution of 4.0 gms of this liquid in 240 ml of methanol is added 0.40 gms of p-toluenesulfonic acid and the reaction is stirred at room temperature for 16 hours. The methanol is removed under reduced pressure, and the residue is partitioned between ethyl acetate and water. The organic layer is washed with aqueous NaHCO3 and brine, then dried over Na2SO4, filtered, and concentrated under vacuum to give 8-(3-methylpentyloxy)octanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05412137 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-4365ea31456546e198c66696939c2a4c |
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| Quellennotiz | uspto-grants-1995_05 |
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