HRID1078748

反应详情

EQUATION

反应方程式

HRID 1078748 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 4.72 g of α-(3,4-dimethoxyphenyl)-1,3-dihydro-α-[(4-methylphenyl)thio]-1,3-dioxo-2H-isoindole-2-heptanenitrile, 100 mL of ethyl alcohol, and 7.0 mL of hydrazine hydrate is heated under reflux. In about a 30 minutes, a heavy precipitate forms. After 1.33 hours, the reaction is cooled to room temperature and concentrated in vacuo. The residue is warmed on a steam bath with 2N hydrochloric acid for 10 minutes. Diatomaceous silica and chloroform are added, the mixture is shaken thoroughly and then filtered through more diatomaceous silica. The organic phase is washed first with aqueous ammonia, then brine, and, after drying (sodium sulfate), it is concentrated in vacuo to give 3.97 g of the desired product as a yellow oil.

WORKUP

后处理

  1. temperatureis heated
  2. temperatureunder reflux
  3. customIn about a 30 minutes
  4. concentrationconcentrated in vacuo
  5. temperatureThe residue is warmed on a steam bath with 2N hydrochloric acid for 10 minutes
  6. additionDiatomaceous silica and chloroform are added
  7. filtrationfiltered through more diatomaceous silica
  8. washThe organic phase is washed first with aqueous ammonia
  9. dry with materialbrine, and, after drying (sodium sulfate), it
  10. concentrationis concentrated in vacuo