HRID36066

反应详情

EQUATION

反应方程式

HRID 36066 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a mixture of 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.39 g of potassium t-butoxide, and 5 ml of dried N,N-dimethylformamide was added dropwise a mixture of 0.42 g of phenyl isocyanate and 1.5 ml of dried N,N-dimethylformamide while stirring under cooling with ice. After stirring for 4 hours under ice-cooling, ice-water was added thereto, and the mixture was made acidic with acetic acid and extracted with diethyl ether. The ether layer was washed with water and dried over sodium sulfate. Diethyl ether was removed by distillation, and the residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.17 g of N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamide represented by formula shown below.

WORKUP

后处理

  1. additionwas added dropwise
  2. temperatureunder cooling with ice
  3. stirringAfter stirring for 4 hours under ice-
  4. temperaturecooling
  5. extractionextracted with diethyl ether
  6. washThe ether layer was washed with water
  7. dry with materialdried over sodium sulfate
  8. customDiethyl ether was removed by distillation
  9. customthe residue was purified by silica gel column chromatography (developing solution: CH2Cl2)