Reaktion #9671

ord-d12c540085124d09aa48e1da1b1b4a13

Reaktionsgleichung

O=S(=O)(Cl)Cl
sulfuryl chloride
O=S(=O)(Cl)Cl
Sulfuryl chloride
FC(F)(F)c1ccc2sc(S)nc2c1
2-mercapto-5-(trifluoromethyl)benzothiazole
FC(F)(F)c1ccc2sc(Cl)nc2c1
2-chloro-5-(trifluoromethyl)benzothiazole
Ausbeute 94.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe product was then extracted with ethyl acetate
  2. 2
    WaschenThe organic layer was washed with water (3×) and brine
  3. 3
    Trocknendried over anhydrous Na2SO4
  4. 4
    Einengenconcentrated
  5. 5
    workup.DISSOLUTIONThe resulting solid was dissolved in EtOAc
  6. 6
    Filtrationfiltered though a short silica-gel column
  7. 7
    Wascheneluting with EtOAc

Vorschrift

Sulfuryl chloride (9.09 g, 67.33 mmol) was added with stirring to 2-mercapto-5-(trifluoromethyl)benzothiazole (2.64 g, 11.22 mmol) over a period of 5 minutes. The reaction mixture was then allowed to stand for approximately 1 h. Ice water was added to the reaction mixture with stirring to decompose the excess of sulfuryl chloride, and the product was then extracted with ethyl acetate. The organic layer was washed with water (3×) and brine, dried over anhydrous Na2SO4 and concentrated. The resulting solid was dissolved in EtOAc and filtered though a short silica-gel column, eluting with EtOAc, to give 2-chloro-5-(trifluoromethyl)benzothiazole (2.50 g, 94%). LC-MS m/z 238.0 (MH+), ret. time 2.55 min; 1H NMR (400 MHz, DMSO-d6) δ 7.81 (d, 1H), 8.38 (m, 2H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091228B2uspto-grants-2006_08