Butyl bromide → 4-Bromo-1-butoxy-2-fluorobenzene

HRID 2068451

Reaktionsgleichung

Reaktionsgleichung von HRID 2068451
[OH-].[Na+].[Br:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([F:11])[CH:5]=1.Br[CH2:13][CH2:14][CH2:15][CH3:16]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:13][CH2:14][CH2:15][CH3:16])=[C:6]([F:11])[CH:5]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Sodium hydroxide (20.2 g) was added to a water (400 ml) solution of 4-bromo-2-fluorophenol (T-7) (76.4 g), bromobutane (65.8 g) and tetrabutylammonium bromide (TBAB) (6.44 g), and the mixture was heated with stirring at 80° C. for 6 hours under an atmosphere of nitrogen. After the completion of the reaction, the reaction mixture was extracted with heptane, and the organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure to leave a black oil. The oil was purified by distillation to give 4-bromo-1-butoxy-2-fluorobenzene (T-8) as a colorless oil (97.5 g) in 98% yield.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. customAfter the completion of the reaction
  3. extractionthe reaction mixture was extracted with heptane
  4. washthe organic layer was washed with water and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationThe solution was concentrated under reduced pressure
  7. customto leave a black oil
  8. distillationThe oil was purified by distillation

Quellen und Nachweise

ORD-Eintrag
ord-c6198ca4fe1649789b46752ecb41c113
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08298632B2

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