Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Peracetic Acid | HCID 6585 | — |
| Edukt | Trimethyl borate | HCID 8470 | — |
| Edukt | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-Bromo-6-chloro-2-fluorophenol | HCID 66601002 | 63% |
Reaktionsschritte
A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in tetrahydrofuran (THF; 50 mL) was slowly added to lithium diisopropylamide (LDA; 0.125 mol) in THF (600 mL) at −50° C. After addition, the solution was warmed to −20° C. and then cooled to −50° C. A solution of trimethyl borate (13.5 g, 0.130 mol) in THF (20 mL) was added slowly and the temperature was warmed to −20° C. The mixture was then cooled to −70° C. and a solution of peracetic acid (32% in acetic acid, 0.150 mol) was slowly added and the mixture was warmed to ambient temperature. Water (250 mL) was added and the solution was extracted with ethyl acetate (2×200 mL). The combined organic phases were dried and concentrated. The black oil was purified by column chromatography (20% ethyl acetate in hexanes) to give 3-bromo-6-chloro-2-fluorophenol (14.1 g, 0.063 mol) 1H NMR (CDCl3): δ 7.05 (m, 2H), 5.5 (br s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07538214B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-18a3d36067c548a8b93a25d7a9dd5ea2 |
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| Quellennotiz | uspto-grants-2009_05 |
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