Реакция #586142

ord-4d56f78854aa46868128c4d24efb12ee

Уравнение реакции

N#Cc1ccc(-c2ccc(C(F)(F)F)cc2)cc1F
2-fluoro-4-(4-trifluoromethylphenyl)benzonitrile
CS.[Na]
sodium methyl mercaptan
CSc1cc(-c2ccc(C(F)(F)F)cc2)ccc1C#N
2-methylthio-4-(4-trifluoromethylphenyl)benzonitrile
Выход 75.4%

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with 100 ml of ethyl acetate twice
  2. 2
    ПромывкаThe ethyl acetate layer was washed with 100 ml of water twice
  3. 3
    Сушкаdried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
  5. 5
    ДругоеPurification of the residue by silica gel column chromatography

Методика

To 3.0 g (11.3 mmol) of 2-fluoro-4-(4-trifluoromethylphenyl)benzonitrile in 50 ml of N,N-dimethylformamide, 7.0 g (15.0 mmol) of 15% aqueous sodium methyl mercaptan was added dropwise at room temperature. After 6 hours of stirring at 60° C., the reaction mixture was poured into 200 ml of ice-cold water and extracted with 100 ml of ethyl acetate twice. The ethyl acetate layer was washed with 100 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 2.5 g of 2-methylthio-4-(4-trifluoromethylphenyl)benzonitrile (yield 75%) as white crystals (m.p. 128-129° C.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07767626B2uspto-grants-2010_08