Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | 1,5-Pentanediol | HCID 8105 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-(Benzyloxy)pentan-1-ol | HCID 221194 | 56,8% |
Reaktionsschritte
A stirred solution of 107.0 grams (1.0 mole) of 1,5-pentanediol, 30 ml (0.25 mole) of phenylmethyl bromide and 33.0 grams of 85% potassium hydroxide in 40 ml of xylenes was heated at 110° C. for 18 hours. After this time the reaction mixture was cooled and shaken with diethyl ether and water. The organic layer was washed in turn with water, aqueous 5% hydrochloric acid, water, and with an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residual oil. The oil was subjected to column chromatography on silica gel. Elution was accomplished using 0.5-50% diethyl ether in hexanes. The appropriate fractions were combined and concentrated under reduced pressure yielding 27.6 grams of 7-phenyl-6-oxaheptan-1-ol. The nmr spectrum was consistent with the proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05081287 |
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| Quelldatensatz | uspto-grants-1992_01 |
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| ORD ID | ord-de1f41e7ed32489f99bd398ddfcde193 |
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| Quellennotiz | uspto-grants-1992_01 |
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