HRID35705

反应详情

EQUATION

反应方程式

HRID 35705 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

1-Acetyl-1-(4-chlorophenyl)cyclobutane (61 g prepared in a similar manner to that described in Example 1 for 1-acetyl-1-(3,4-dichlorophenyl)cyclobutane, platinum oxide (0.75 g), 33% solution of methylamine in ethanol (60 g) and ethanol (30 ml) were charged into an autoclave. The autoclave was filled with hydrogen and maintained at about 60° C. and 20 bar pressure for ten hours. The reaction mixture was filtered through charcoal and the solids washed with absolute alcohol. The solvents were removed by evaporation and a sample of the residue (10 g) was shaken with 2M hydrochloric acid (50 ml) and ether (50 ml). The aqueous layer was basified and extracted with ether. The ether extract yielded a liquid on evaporation which was distilled (109° C./0.3 mm Hg) to give N-methyl-1-[1-(4-chlorophenyl)cyclobutyl]ethylamine (Formula I R1 =Me; R2 =H; R3 =Me; R4 =H; R5 =4--Cl and R6 =H).

WORKUP

后处理

  1. additionwere charged into an autoclave
  2. wait20 bar pressure for ten hours
  3. filtrationThe reaction mixture was filtered through charcoal
  4. washthe solids washed with absolute alcohol
  5. customThe solvents were removed by evaporation
  6. extractionextracted with ether
  7. extractionThe ether extract
  8. customyielded a liquid
  9. customon evaporation which
  10. distillationwas distilled (109° C./0.3 mm Hg)