反応 #55442

ord-e0e102ed6dc546d8920f4a44faf3a4e8

反応方程式

COc1ccc(CCN)cc1OC
3,4-Dimethoxyphenethylamine
Cc1ccc(NCC(=O)O)cc1
p-toluidinoacetic acid
COc1ccc(CCNC(=O)CNc2ccc(C)cc2)cc1OC
N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamide
収率 71.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling
  2. 2
    洗浄the solution was washed with a cooled 1 N sodium hydroxide solution and water
  3. 3
    その他dried
  4. 4
    workup.DISTILLATIONThe solvent was distilled off
  5. 5
    その他the oily residue was crystallized
  6. 6
    workup.ADDITIONby adding ether

実験手順

3,4-Dimethoxyphenethylamine (14.4 g ) and p-toluidinoacetic acid (13.1 g) were heated for 1.5 hours at 190° C. in a stream of nitrogen. After cooling, the reaction mixture was dissolved in ethyl acetate and the solution was washed with a cooled 1 N sodium hydroxide solution and water and then dried. The solvent was distilled off and the oily residue was crystallized by adding ether to give N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamide (18.6 g), mp 87° to 88.5° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04220647uspto-grants-1980_09