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
PROCEDURE
实验过程
A mixture of 8.3 parts of ethyl [2-[[4-[(4-chlorophenyl)cyanomethyl]-3-methoxyphenyl]hydrazono]-2-cyanoacetyl]carbamate, 1.77 parts of anhydrous potassium acetate and 100 parts of acetic acid is stirred for 2 hours at reflux temperature. The reaction mixture is evaporated in vacuo. The residue is stirred in water. The product is filtered off and dissolved in trichloromethane. The organic layer is dried, filtered and evaporated. The residue is purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated in vacuo, yielding 2-[4-[(4-chlorophenyl)cyanomethyl]-3-methoxyphenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carbonitrile.
WORKUP
后处理
- temperatureat reflux temperature
- customThe reaction mixture is evaporated in vacuo
- stirringThe residue is stirred in water
- filtrationThe product is filtered off
- dissolutiondissolved in trichloromethane
- customThe organic layer is dried
- filtrationfiltered
- customevaporated
- customThe residue is purified by column chromatography over silica gel using
- additiona mixture of trichloromethane and methanol (90:10 by volume) as eluent
- customThe pure fractions are collected
- customthe eluent is evaporated in vacuo