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
- 0 °C
PROCEDURE
实验过程
In a 3-necked 50 ml flask fitted with a sintered glass gas inlet tube, 2.13 g (0.0135 mol) of 4-p-tolyl-but-3-enenitrile are dissolved in 30 ml of methanol, and cooled to 0° C. Sodium hydroxide (0.54 g; 0.0135 mol) is added. The turbid, slightly brownish mixture is then treated with ca. 0.025 mol of gaseous methyl nitrite bubbled below the surface of the mixture through the gas inlet tube (methyl nitrite is generated by dropwise addition of [0.8 ml of H2SO4 conc+1.6 ml H2O] to a suspension of sodium nitrite (1.72 g; 0.025 mol) in 3 ml of methanol:water 1:1 (v:v); see M. Itoh et al. Org. Synth. Coll vol. VI, 1988, 199). The mixture is then stirred overnight, allowing the temperature to rise to 25° C. The solvent is evaporated in vacuo, the residue is redissolved in water and extracted with toluene. The aqueous phase is then acidified with conc. HCl to pH ca 2, the beige precipitate is filtered, rinsed neutral with water, and dried under vacuum. The crude product is redissolved in ethyl acetate, filtered through a short pad of SiO2, and evaporated. 2-Hydroxyimino-4-p-tolyl-but-3-enenitrile (1.9 g; 76%), mp 135-137° C. is obtained and used without further purification.
WORKUP
后处理
- customIn a 3-necked 50 ml flask fitted with a sintered glass gas inlet tube
- custombubbled below the surface of the mixture through the gas inlet tube (methyl nitrite
- customto rise to 25° C
- customThe solvent is evaporated in vacuo
- dissolutionthe residue is redissolved in water
- extractionextracted with toluene
- filtrationthe beige precipitate is filtered
- washrinsed neutral with water
- customdried under vacuum
- dissolutionThe crude product is redissolved in ethyl acetate
- filtrationfiltered through a short pad of SiO2
- customevaporated