HRID1029768

反应详情

EQUATION

反应方程式

HRID 1029768 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

A 1.6 M solution of butyllithium in hexane (19.0 ml. 28 mmol) was added to a stirred solution of diisopropylamine (3.9 ml, 28 mmol) in dry ether (40 ml) at -70° C. under argon, and the resulting solution was stirred at -70° C. for 45 minutes. A solution of 2-cyanothiophene (2.6 ml, 28 mmol) in dry ether (10 ml) was then added. The mixture was stirred at -70° C, for 1 hour, then sulphur (1.27 g, 28 mmol) was added slowly at -50° C. After stirring the mixture at -50° C. for 1 hour, it was allowed to warm to ambient temperature and then stirred for a further 30 minutes. The resultant mixture, containing the lithium salt of 5-cyanothiophene-2-thiol, was diluted with ether (100 ml) and a solution of sodium hydroxide (1.68 g, 42 mmol) in water (100 ml) was added. Nitromethane (1.54 ml, 28 mmol) was then added to the vigorously stirred mixture followed by powdered potassium ferricyanide (9.34 g, 56 mmol), and the resultant mixture was stirred at ambient temperature for 1 hour. The mixture was filtered through diatomaceous earth to remove insoluble matter and the aqueous phase was separated and acidified to pH 1with 28% hydrochloric acid. The mixture was extracted with ethyl acetate, dried (MgSO4), and the solvent was removed by evaporation. The resultant oil (2.6 g) was purified by flash chromatography (Merck Kieselgel Art 9385) using ethyl acetate/hexane (1:4 v/v), to give 5-cyano-2-(nitromethylthio)thiophene as an oil (0.5 g, 10% yield); NMR: 5.4(s,2H), 7.4(q,2H).

WORKUP

后处理

  1. stirringThe mixture was stirred at -70° C, for 1 hour
  2. stirringAfter stirring the mixture at -50° C. for 1 hour
  3. temperatureto warm to ambient temperature
  4. stirringstirred for a further 30 minutes
  5. filtrationThe mixture was filtered through diatomaceous earth
  6. customto remove insoluble matter
  7. customthe aqueous phase was separated
  8. extractionThe mixture was extracted with ethyl acetate
  9. dry with materialdried (MgSO4)
  10. customthe solvent was removed by evaporation
  11. customThe resultant oil (2.6 g) was purified by flash chromatography (Merck Kieselgel Art 9385)