Реакция #9671

ord-d12c540085124d09aa48e1da1b1b4a13

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияthe product was then extracted with ethyl acetate
  2. 2
    ПромывкаThe organic layer was washed with water (3×) and brine
  3. 3
    Сушкаdried over anhydrous Na2SO4
  4. 4
    Концентрированиеconcentrated
  5. 5
    workup.DISSOLUTIONThe resulting solid was dissolved in EtOAc
  6. 6
    Фильтрацияfiltered though a short silica-gel column
  7. 7
    Промывкаeluting with EtOAc

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091228B2uspto-grants-2006_08