Réaction #1457781

ord-dde246ed10664faf9b7ae3be31c59a55

Équation de réaction

O=S(=O)(Cl)c1c(F)c(F)c(F)c(F)c1F
C6F5SO2Cl
Cc1cccc(C)n1
2,6-lutidine
O=S(=O)(Cl)Cl
sulfonyl chloride
Cc1cccc(C)n1.Cl
2,6-lutidine hydrochloride

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.DISSOLUTIONonly partly dissolved)
  2. 2
    workup.ADDITIONDuring the addition
  3. 3
    workup.DISSOLUTIONthe starting material dissolved

Mode opératoire

Aniline 9.3 (44.6 g, 268 mmol) and 2,6-lutidine (32.8 mL, 282 mmol) were dissolved in 800 mL of acetone (the aniline only partly dissolved). An addition funnel was charged with C6F5SO2Cl (41.8 mL, 282 mmol) and the sulfonyl chloride was added over 15 minutes. During the addition, the starting material dissolved and a new precipitate (2,6-lutidine hydrochloride) formed. After 30 minutes, the 2,6-lutidine hydrochloride was removed by filtration and the filtrate concentrated under reduced pressure. The brown oily solid so produced was triturated with CH2Cl2 and the solid collected. A second batch of product was obtained by repeating the concentration, trituration, and filtration. After drying under high vacuum, 95.5 g (90%) of sulfonamide 9.4 was obtained as a pale yellow solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06583165B2uspto-grants-2003_06