Reaktion #95564

ord-f0ca0e9fafa44133964a201cb876e151

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe precipitated pyridine hydrochloride was filtered
  2. 2
    Waschenwashed with benzene
  3. 3
    Waschenwashed
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    Sonstigeto remove any acid
  6. 6
    Sonstigea rotary evaporator

Vorschrift

106 g (0.6 mole) of pelargonoyl chloride was added dropwise with stirring to a solution of 32.6 g (0.2 mole) of N,N-bis(hydroxyethyl)hydroxyacetamide in 60 ml of pyridine. The precipitated pyridine hydrochloride was filtered, washed with benzene, and discarded. The benzene solution of product was water washed, dried over sodium sulfate, and passed through an activated alumina column to remove any acid. The benzene was stripped off an a rotary evaporator. The yield of product was essentially quantitative. Its structure was established by infrared and nuclear magnetic resonance spectroscopy. It had nD30 1.4537 and d430 0.9745.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346043uspto-grants-1982_08