反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- stirringThe mixture was stirred at -70° C, for 1 hour
- stirringAfter stirring the mixture at -50° C. for 1 hour
- temperatureto warm to ambient temperature
- stirringstirred for a further 30 minutes
- filtrationThe mixture was filtered through diatomaceous earth
- customto remove insoluble matter
- customthe aqueous phase was separated
- extractionThe mixture was extracted with ethyl acetate
- dry with materialdried (MgSO4)
- customthe solvent was removed by evaporation
- customThe resultant oil (2.6 g) was purified by flash chromatography (Merck Kieselgel Art 9385)