Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Benzenemethanol, 3-bromo-, 1-acetate | HCID 12858554 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | Benzenemethanol, 3-phenoxy-, 1-acetate | HCID 170904 | 77% |
Reaktionsschritte
10.35 g. (0.11 mole) of phenol, 6.15 g. (0.11 mole) of potassium hydroxide and 35 cm3. of xylene are weighed together. The water is azeotropically distilled with stirring and boiling. 5 cm3. of pyridine and 0.5 g. of copper(I) chloride are added then 22.91 g. (0.1 mole) of 3-bromobenzyl acetate are dropped into the reaction mixture during 15 minutes with stirring and boiling. The reaction mixture is boiled with stirring for an additional three hours. After cooling the reaction mixture is filtered off and the filtrate washed with a mixture of 25 cm3. of 15% sodium chloride solution and 2 cm3. of 40% sodium hydroxide solution. The organic phase is evaporated in vacuo. The residue is distilled in vacuo and so 18.65 g. of 3-phenoxybenzyl acetate are obtained. Boiling point 142°-145° C./53.2 Pa, nD20 : 1.5621, yield 77%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04709081 |
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| Quelldatensatz | uspto-grants-1987_11 |
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| ORD ID | ord-9324d319bedd4b14a18344d4054d26d2 |
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| Quellennotiz | uspto-grants-1987_11 |
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