反应 #49656

ord-78f7e330337c40a8bdfa74f1db69078a

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONWhen addition
  2. 2
    温度heated
  3. 3
    温度to reflux for 3 hours
  4. 4
    温度cooled
  5. 5
    其他The mixture was then evaporated on a rotary evaporator at 60° for 1/2 hour
  6. 6
    萃取extracted with CH2Cl2 (3×25 ml)
  7. 7
    洗涤The combined extracts were washed with water
  8. 8
    干燥dried (MgSO4)
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    过滤filtered
  10. 10
    其他evaporated

实验过程

A solution of N-butyl-4-chlorobenzamide (2.26 g; 0.011 mol) in dry THF (25 ml) was added slowly to an ice-cooled solution of 1.0M B2H6 --THF complex (45 ml; 0.045 tool) under a nitrogen blanket. When addition was complete, the mixture was stirred and heated to reflux for 3 hours, cooled and decomposed by dropwise addition of 1:1 conc aq HCl-water (10 ml). The mixture was then evaporated on a rotary evaporator at 60° for 1/2 hour to decompose the boron-amine complexes. The residue was taken up in water, strongly basified with aq NaOH and extracted with CH2Cl2 (3×25 ml). The combined extracts were washed with water, dried (MgSO4), filtered and evaporated to give n-butyl-4-chlorobenzenemethanamine (1.79 g) as an oil. The oil was converted to the hydrochloride salt of the title compound (1.98 g) by crystallising from ethanolic HCl and ethyl acetate, mp 250°-252° after melting and resolidifying at 203°-207° .

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05422355uspto-grants-1995_06