N-methyl-2-pyrrolidone → 4-Bromo-3-chloro-3,4,4-trifluorobutan-1-ol

HRID 439672

Reaktionsgleichung

Reaktionsgleichung von HRID 439672
[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5]Br.CN1CCCC1=[O:17]>O>[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5][OH:17]

Komponenten

4

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

A mixture of 1,4-dibromo-2-chloro-1,1,2-trifluorobutane (XVI) (7.5 g, 24.6 mmol), 1-methyl-2-pyrrolidinone (14 mL) and water (2.5 mL) was heated at 130° C. for 16 hours. The mixture was cooled to room temperature, diluted with water (80 mL) and extracted with ether (2×75 mL). The ether extract was washed with water (31×40 mL), brine, and dried over anhydrous magnesium sulfate. The residue obtained after evaporation of the solvent was chromatographed over silica gel to give 2.9 g (49%) of the desired alcohol as a clear oil.

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. extractionextracted with ether (2×75 mL)
  3. extractionThe ether extract
  4. washwas washed with water (31×40 mL), brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe residue obtained
  7. customafter evaporation of the solvent
  8. customwas chromatographed over silica gel

Quellen und Nachweise

ORD-Eintrag
ord-d50b6a50e67449de839290b11556f0b4
Quelldatensatz
uspto-grants-1996_05
Patentnummer
US05514717

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