Реакция #9670

ord-661e57de66044a9898eced4c290b9652

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was then heated at 140° C. for 6 hours
  2. 2
    ТемператураAfter cooling the solution to rt
  3. 3
    Другоеthe product was precipitated by addition of conc. HCl
  4. 4
    Фильтрацияcollected by filtration
  5. 5
    Другоеrecrystallized from isopropyl ether

Методика

To a mixture of sodium hydride (0.98 g, 40.91 mmol) and diethylene glycol monoethyl ether (25 mL) was added 2-chloro-5-(trifluoromethyl)aniline (5.00 g, 25.57 mmol) under a nitrogen atmosphere. The resulting mixture was stirred at rt for 30 minutes, and then carbon disulfide (3.89 g, 51.13 mmol) was added. The reaction mixture was then heated at 140° C. for 6 hours. After cooling the solution to rt, the product was precipitated by addition of conc. HCl, collected by filtration, and recrystallized from isopropyl ether to afford 2-mercapto-5-(trifluoromethyl)benzothiazole (2.65 g, 44%). 1H NMR (400 MHz, DMSO-d6) δ 7.49 (s, 1H), 7.61 (d, 1H), 7.94 (d, 1H).

Источник

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