Peracetic Acid → 3-Bromo-6-chloro-2-fluorophenol

HRID 495015

Reaktionsgleichung

Reaktionsgleichung von HRID 495015
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[F:9].C([N-]C(C)C)(C)C.[Li+].B(OC)(OC)[O:19]C.C(OO)(=O)C>O1CCCC1.O>[Br:1][C:2]1[C:3]([F:9])=[C:4]([OH:19])[C:5]([Cl:8])=[CH:6][CH:7]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

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).

Aufarbeitung

  1. additionAfter addition
  2. temperaturecooled to −50° C
  3. temperaturethe temperature was warmed to −20° C
  4. temperatureThe mixture was then cooled to −70° C.
  5. temperaturethe mixture was warmed to ambient temperature
  6. extractionthe solution was extracted with ethyl acetate (2×200 mL)
  7. customThe combined organic phases were dried
  8. concentrationconcentrated
  9. customThe black oil was purified by column chromatography (20% ethyl acetate in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-18a3d36067c548a8b93a25d7a9dd5ea2
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07538214B2

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