(Diethylamino)sulfur trifluoride → 1-fluoro-3-(2,4,6-trichloro-phenyl)-propan-2-one O-methyl-oxime

HRID 1039348Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1039348
[CH3:1][O:2][N:3]=[C:4]([CH2:7][C:8]1[C:13]([Cl:14])=[CH:12][C:11]([Cl:15])=[CH:10][C:9]=1[Cl:16])[CH2:5]O.C(N(S(F)(F)[F:23])CC)C>ClCCl>[CH3:1][O:2][N:3]=[C:4]([CH2:7][C:8]1[C:13]([Cl:14])=[CH:12][C:11]([Cl:15])=[CH:10][C:9]=1[Cl:16])[CH2:5][F:23]

Komponenten

4

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a stirred brown suspension of 1-hydroxy-3-(2,4,6-trichloro-phenyl)-propan-2-one O-methyl-oxime (33 g; 117 mmol) in dichloromethane (235 ml) at −20° C. under nitrogen was added dropwise a solution of diethylaminosulfur trifluoride (16 ml; 123 mmol) in dichloromethane (62 ml). During addition, temperature rose to −10° C. The mixture turned to a brown orange solution which was allowed to warm at 20° C. and was stirred for 2 hours. The organic solution was washed with saturated hydrogen carbonate solution (200 ml), 1N hydrochloric acid (200 ml), brine (200 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 37 g (110% of theory) of crude 1-fluoro-3-(2,4,6-trichloro-phenyl)-propan-2-one O-methyl-oxime (isomers E/Z) as a brown oil.

Aufarbeitung

  1. additionDuring addition, temperature
  2. customrose to −10° C
  3. washThe organic solution was washed with saturated hydrogen carbonate solution (200 ml), 1N hydrochloric acid (200 ml), brine (200 ml)
  4. dry with materialdried over sodium sulfate
  5. customThe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-225899cc8f5143a88ceb5d113038e135
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08552049B2

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