Réaction #3058

ord-428799f362c448f9a4b5974ac3fa405b

Équation de réaction

NC1CCCCCC1
cycloheptylamine
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C(Br)CBr
bromoacetyl bromide
O=C(CBr)NC1CCCCCC1
solid
Rendement 89.7%
O=C(CBr)NC1CCCCCC1
Bromo-N-cycloheptyl acetamide
Rendement 89.7%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreTo a -20° C.
  2. 2
    workup.STIRRINGstirred for an additional 30 minutes
  3. 3
    AutreThe organic layer was separated
  4. 4
    Lavagewashed with water (3×100 mL)
  5. 5
    Séchagedried over magnesium sulfate
  6. 6
    Concentrationconcentrated in vacuo

Mode opératoire

To a -20° C. solution of cycloheptylamine (6.37 mL, 50.0 mmol) and diisopropylethylamine (9.58 mL, 55.0 mmol) in methylene chloride (250 mL) was slowly added bromoacetyl bromide (4.78 mL, 55.0 mmol). The reaction mixture was warmed to room temperature over 20 minutes and stirred for an addition 30 minutes. The reaction mixture was diluted with water (100 mL) and stirred for an additional 30 minutes. The organic layer was separated, washed with water (3×100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (10.5 g). The crude material was further purified by silica gel flash column chromatography using hexane-ethyl acetate (1:1) as the eluent to give the purified title compound as a whim solid (9.77 g, 83%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05731438uspto-grants-1998_03