Реакция #50546

ord-e11ad11d2499429e80643360e0a1b5f0

Уравнение реакции

Sc1cccc(Br)c1
3-Bromothiophenol
C=CC#N
acrylonitrile
N#CCCSc1cccc(Br)c1
3-[(3-bromophenyl)thio]propionitrile
Выход 93.7%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONTriton B (1 mL) was added, at which time the reaction mixture
  2. 2
    Температураto reflux
  3. 3
    workup.ADDITIONwithout added
  4. 4
    Температураheat
  5. 5
    Экстракцияextracted with diethyl ether
  6. 6
    ДругоеThe organic layer was dried
  7. 7
    Фильтрацияfiltered
  8. 8
    Другоеevaporated

Методика

3-Bromothiophenol (10 g, 52.9 mmmol) was dissolved in acrylonitrile (11.28 g, 213 mmol). Triton B (1 mL) was added, at which time the reaction mixture became exothermic and began to reflux without added heat. The mixture was allowed to cool to room temperature, poured into cold aqueous sodium hydroxide (2%; 200 mL), and extracted with diethyl ether. The organic layer was dried, filtered and evaporated to provide 12 g (93%) of 3-[(3-bromophenyl)thio]propionitrile as a tan oil; 1H NMR (CDCl3) δ7.54 (s, 1H), 7.42 (d, 1H), 7.32 (d, 1H), 7.25-7.15 (m, 2H), 3.15 (t, 2H), 2.62 (t, 2H); Mass spectrum m/z 261, 259 (M+NH4).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05428040uspto-grants-1995_06