Dichloromethane → 2-fluoro-N-hydroxybenzenecarboximidoyl chloride

HRID 1196579

Reaction equation

HRID 1196579 reaction equation
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[CH:4]=[N:5][OH:6].[Cl:11]CCl>>[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([Cl:11])=[N:5][OH:6]

Participants

3

Conditions

Temperature
-10 °C

Procedure

In 1 liter dichloromethane was dissolved 55.0 g 2-fluorobenzaldehyde oxime at room temperature with stirring. The resulting solution was cooled to -10° C. and Cl2 was bubbled in at such a rate to maintain temperature below 15° C. After a dark blue color was generated (2-3 minutes) a solution of triethylamine (50 ml) in dichloromethane (100 ml) was added dropwise concurrently with Cl2 addition. When the reaction mixture had maintained a yellow color, additions of the triethylamine solution and Cl2 were discontinued. Concentration of the reaction mixture left an oil which was dissolved in ether and washed four times with 3N HCl followed by a final wash with brine. The organic layer was dried (MgSO4), filtered and concentrated in vacuo to give 60.0 g of 2-fluoro-N-hydroxybenzenecarboximidoyl chloride as an oil which solidified on standing.

Workup

  1. customCl2 was bubbled in at such a rate
  2. temperatureto maintain temperature below 15° C
  3. custom(2-3 minutes)
  4. additionwas added dropwise concurrently with Cl2 addition
  5. temperatureWhen the reaction mixture had maintained a yellow color, additions of the triethylamine solution and Cl2
  6. waitConcentration of the reaction mixture left an oil which
  7. dissolutionwas dissolved in ether
  8. washwashed four times with 3N HCl
  9. washa final wash with brine
  10. dry with materialThe organic layer was dried (MgSO4)
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-cf8b7427b68b4260ba67f9feb78b7119
Source dataset
uspto-grants-1992_05
Patent number
US05114936

Linked notes

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