Reaction #55336

ord-e92d68471f384dd693101c367d0b9ebe

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ConcentrationThe reaction mixture was concentrated and to the residue
  2. 2
    workup.ADDITIONwas added 1 N NaOH aqueous solution
  3. 3
    FiltrationThe resultant crystals were filtered
  4. 4
    Washwashed well with water
  5. 5
    Otherrecrystallized from ethanol

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04220603uspto-grants-1980_09