Reaktion #5592

ord-0c853584f40147fcac7748a5dc4bc09f

Reaktionsgleichung

CCN(CC)CC
triethylamine
NC12CCCC(C1)C2
norpinylamine
CCOCC
ethyl ether
C=CC(=O)Cl
acryloyl chloride
CCOCC
ethyl ether
C=CC(=O)NC1CCC2CC1C2(C)C
title product
C=CC(=O)NC1CCC2CC1C2(C)C
N-(6,6-dimethylbicyclo[3.1.1]hept-2-yl)-2-propenamide

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe light tan solid was filtered
  2. 2
    Waschenwashed well with ethyl ether
  3. 3
    SonstigeThe solvent and triethylamine were removed

Vorschrift

Following the procedure of Example 3, a solution of acryloyl chloride (4.05 ml, 0.05 mole) in ethyl ether (50 ml) was added dropwise to a cold 5° C. mixture of triethylamine (15.3 ml, 0.11 mole) and norpinylamine (6.96; g, 0.05 mole) in ethyl ether (400 ml). The reaction was allowed to warm to room temperature and stirred for 72 hours. The light tan solid was filtered and washed well with ethyl ether. The solvent and triethylamine were removed, leaving the title product as an oily solid. The structure was confirmed by NMR.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244899uspto-grants-1993_09