반응 #55336

ord-e92d68471f384dd693101c367d0b9ebe

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The reaction mixture was concentrated and to the residue
  2. 2
    workup.ADDITIONwas added 1 N NaOH aqueous solution
  3. 3
    여과The resultant crystals were filtered
  4. 4
    세척washed well with water
  5. 5
    기타recrystallized from ethanol

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04220603uspto-grants-1980_09