Reaktion #7061

ord-a67ac309ad074910a843d2a272c82903

Reaktionsgleichung

CSc1cc(S(N)(=O)=O)sc1[Si](C)(C)C
5-trimethylsilyl-4-methylsulfanylthiophene-2-sulfonamide
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
tetra-butylammonium fluoride
CSc1csc(S(N)(=O)=O)c1
title compound
Ausbeute 82.0%
CSc1csc(S(N)(=O)=O)c1
4-Methylsulfanylthiophene-2-sulfonamide
Ausbeute 82.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe THF is removed under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue is dissolved in EtOAc (200 mL)
  3. 3
    WaschenThe organic layer is washed with brine
  4. 4
    Trocknenthen dried (Na2SO4)
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    SonstigeThe crude product is chromatographed on silica gel
  8. 8
    Wascheneluting with Hex

Vorschrift

To a solution of 5-trimethylsilyl-4-methylsulfanylthiophene-2-sulfonamide (660 mg, 2.34 mmol) in THF (10 mL) is added a solution of tetra-butylammonium fluoride (14.0 mL of 1 M in THF, 14.0 mmol). The reaction mixture is stirred at room temperature for 3 hr. The THF is removed under reduced pressure and the residue is dissolved in EtOAc (200 mL). The organic layer is washed with brine then dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with Hex:EtOAc (2:1) to afford the title compound (400 mg, 82%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084170B2uspto-grants-2006_08