Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene carbonate | HCID 7303 | — |
| Edukt | 4-Bromo-2,6-dimethylphenol | HCID 16919 | — |
| Edukt | Lithium hydride | HCID 62714 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(4-Bromo-2,6-dimethylphenoxy)ethanol | HCID 53707443 | 64,4% |
Reaktionsschritte
Lithium hydride (200 mg) was added to a stirred solution of 4-bromo-2,6-dimethylphenol (65 g) in DMF at ambient temperature. When evolution of hydrogen had ceased, ethylene carbonate (31.9 g) was added and the mixture was heated at 150° C. for 12 hours. The DMF was removed by evaporation and the cooled residue was dissolved in ethyl acetate (500 ml). The ethyl acetate solution was washed with water (2×100 ml) and then with saturated brine (100 ml), dried (MgSO4) and evaporated. The residue was crystallised from methanol to give 2-(4-bromo-2,6-dimethylphenoxy)ethanol (51 g), m.p. 47-48° C. NMR (CDCl3): 2.21(6H,s), 3.86(2H,m), 3.93(2H,m), 7.12(2H,s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05919793 |
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| Quelldatensatz | uspto-grants-1999_07 |
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| ORD ID | ord-06e81898d9a141c3857cc9c903700f23 |
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| Quellennotiz | uspto-grants-1999_07 |
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