HRID64775

反应详情

EQUATION

反应方程式

HRID 64775 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

152 G (1.0 M) of campholenic aldehyde having a purity of about 75% were added dropwise under stirring in 15-20 minutes to a mixture cooled at -5/-10° of 400 g (6.1 M) of methyl-ethyl ketone, 1025 g (35 M) of methanol, 30.5 g (0.54 M) of potassium hydroxide and 380 g of water. The mixture was kept at -5° for 24 hours, then at room temperature for the same period and neutralized thereupon with H2SO4 to 62.5%. After concentration under reduced pressure, the obtained residue was dissolved in 200 ml of water, diluted with petrol ether 30/50, washed until neutrality, dried and concentrated. 189.3 G of a raw material was thus obtained which on distillation with a Vigreux column of 15 cm length gave 144.6 g of (E)-3-methyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-3-penten-2-one having a purity of 86% (yield 60.4%).

WORKUP

后处理

  1. waitThe mixture was kept at -5° for 24 hours
  2. customat room temperature
  3. concentrationAfter concentration under reduced pressure
  4. dissolutionthe obtained residue was dissolved in 200 ml of water
  5. additiondiluted with petrol ether 30/50
  6. washwashed until neutrality
  7. customdried
  8. concentrationconcentrated
  9. custom189.3 G of a raw material was thus obtained which
  10. distillationon distillation with a Vigreux column of 15 cm length