3-Fluoro-3-methylbutan-2-one → 1,1-Dibromo-3-fluoro-3-methyl-2-butanone

HRID 586226Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 586226
[CH3:1][C:2]([F:7])([CH3:6])[C:3](=[O:5])[CH3:4].[Br-:8].[Br-:9].[Br-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>ClCCl>[Br:8][CH:4]([Br:9])[C:3](=[O:5])[C:2]([F:7])([CH3:6])[CH3:1]

Komponenten

4

Versuchsvorschrift

To a stirred solution of 3-methyl-3-fluoro-2-butanone (0.1031 g, 0.990 mmol) in anhydrous dichloromethane (5 ml) under nitrogen was added solid pyridinium tribromide (0.7035 g, 1.98 mmol) and the mixture was stirred at room temperature for 18 h. The mixture was then diluted with dichloromethane (5 ml), washed with dilute aqueous sodium hydrogensulfite (10 ml), then saturated aqueous NaCl (10 ml), dried (Na2SO4) and evaporated under low vacuum with no heat. The residue was purified by flash chromatography [silica gel, 5% Et2O/petroleum ether (40-60° C.)] to afford 0.1869 g (72%) of the title compound as a colourless oil: 1H NMR (360 MHz, CDCl3) δ 1.65 (6H, d, J 21.5 Hz), 6.51 (1H, d, J 1.5 Hz).

Aufarbeitung

  1. washwashed with dilute aqueous sodium hydrogensulfite (10 ml)
  2. dry with materialsaturated aqueous NaCl (10 ml), dried (Na2SO4)
  3. customevaporated under low vacuum with no heat
  4. customThe residue was purified by flash chromatography [silica gel, 5% Et2O/petroleum ether (40-60° C.)]

Quellen und Nachweise

ORD-Eintrag
ord-de16cfa6637a434bad7cdf898ae9d724
Quelldatensatz
uspto-grants-2005_08
Patentnummer
US06936608B2

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