反应 #55336

ord-e92d68471f384dd693101c367d0b9ebe

反应方程式

BrCCOc1ccccc1CCc1ccccc1
2-(2-bromoethoxy)bibenzyl
NC(=O)C1CCNCC1
4-piperidinecarboxamide
NC(=O)C1CCN(CCOc2ccccc2CCc2ccccc2)CC1
2-[2-(4-carbamoylpiperidino)ethoxy]bibenzyl
收率 82.3%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction mixture was concentrated and to the residue
  2. 2
    workup.ADDITIONwas added 1 N NaOH aqueous solution
  3. 3
    过滤The resultant crystals were filtered
  4. 4
    洗涤washed well with water
  5. 5
    其他recrystallized from ethanol

实验过程

A solution of 2 g of 2-(2-bromoethoxy)bibenzyl and 1.7 g of 4-piperidinecarboxamide in 20 ml of tetrahydrofuran and 10 ml of water was stirred at 70° C. for 10 hours. The reaction mixture was concentrated and to the residue was added 1 N NaOH aqueous solution. The resultant crystals were filtered, washed well with water and then recrystallized from ethanol to give 1.9 g (82% yield) of 2-[2-(4-carbamoylpiperidino)ethoxy]bibenzyl, m. p. 60°-63° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04220603uspto-grants-1980_09