HRID1285365

反应详情

EQUATION

反应方程式

HRID 1285365 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

The intermediate 3-amino-1-(2-furanyl)-2-buten-1-one was prepared as follows: A mixture containing 165 g of 1-(2-furanyl)-1,3-butanedione, 700 ml of toluene and 200 g of ammonium acetate was azeotroped for six hours, cooled and concentrated to dryness in vacuo. The residue was dissolved in isopropyl alcohol, the solution treated with decolorizing charcoal and filtered, and the filtrate concentrated to remove the solvent. The remaining residue was recrystallized from ether-ethanol and dried at room temperature to yield 80.2 g of 3-amino-1-(2-furanyl)-2-buten-1-one, m.p. 128°-130° C. Another 33.4 g of the product, m.p. 128°-130° C. was collected by concentrating the mother liquor and extracting the product with ether.

WORKUP

后处理

  1. customThe intermediate 3-amino-1-(2-furanyl)-2-buten-1-one was prepared
  2. customwas azeotroped for six hours
  3. temperaturecooled
  4. concentrationconcentrated to dryness in vacuo
  5. dissolutionThe residue was dissolved in isopropyl alcohol
  6. additionthe solution treated with decolorizing charcoal
  7. filtrationfiltered
  8. concentrationthe filtrate concentrated
  9. customto remove the solvent
  10. customThe remaining residue was recrystallized from ether-ethanol
  11. customdried at room temperature