Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromopentane | HCID 8057 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Bromo-4'-hydroxybiphenyl | HCID 95093 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 4-Bromo-4'-(pentyloxy)-1,1'-biphenyl | HCID 2801388 | 94,9% |
Reaktionsschritte
To a stirred solution of 4-(4-bromophenyl)phenol (25.5 g, 0.102 mol) in 400 mL of dimethylsulfoxide was added 2.5N NaOH (40.9 ml, 0.102 mol) followed by n-pentyl bromide (12.7 mL, 0.102 mol). The resulting mixture was heated at 70° C. for a period of 18 h. After cooling, the yellow solution was partitioned between ethyl acetate (1000 ml) and water (500 ml). The organic phase was washed with water (3×) and brine and dried with magnesium sulfate. The solvent was removed in vacuo to give 4-(4-n-pentoxyphenyl)bromobenzene (30.9 g): 1H NMR (400 MHz, DMSO-d6) δ 0.93 (t, 3, J=7.2 Hz), 1.41 (m, 4), 1.79 (m, 2), 3.97 (t, 2, J=6.6 Hz), 6.94 (d, 2, J=8.8 Hz), 7.39 (d, 2, J=8.6 Hz), 7.45 (d, 2, J=8.8 Hz), 7.51 (d, 2, J=8.6 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05516756 |
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| Quelldatensatz | uspto-grants-1996_05 |
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| ORD ID | ord-f61a057f7cc144d0a6990451e2c57ee6 |
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| Quellennotiz | uspto-grants-1996_05 |
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