Reaktion #51886

ord-c0611c5f8c5b4b40ae10354cd46eeab6

Reaktionsgleichung

N#Cc1cc(F)c(F)c(F)c1
3,4,5-trifluorobenzonitrile
OCCNCCO
diethanolamine
N#Cc1cc(F)c(N(CCO)CCO)c(F)c1
3,5-difluoro-4-[bis(2-hydroxyethyl)amino]benzonitrile

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was then evaporated
  2. 2
    Sonstigethe residue partitioned between CH2Cl2 (200 ml) and H2O (200 ml)
  3. 3
    Trocknenthe organic layer dried (MgSO4)
  4. 4
    Sonstigeevaporated to dryness
  5. 5
    SonstigeThe residue was chromatographed
  6. 6
    Sonstigeto give
  7. 7
    Sonstigeafter recrystallization from toluene, 2.7 g (35%) of pure white crystals

Vorschrift

A solution of 3,4,5-trifluorobenzonitrile (5 g, 32 mmol) and diethanolamine (6 ml, 85 mmol) in N,N-dimethylacetamide was stirred for 10 days. The solvent was then evaporated, the residue partitioned between CH2Cl2 (200 ml) and H2O (200 ml), the organic layer dried (MgSO4) and evaporated to dryness. The residue was chromatographed using CH2Cl2-EtOAc as eluent to give, after recrystallization from toluene, 2.7 g (35%) of pure white crystals: mp 63-65° C.; 1H NMR δ3.33 (t, 4H, NCH2, J=6 Hz), 3.48 (t, 4H, OCH2, J=6 Hz), 4.43 (bs, 2H, OH), 7.57 (dd, 2H, H2+6, JH2, F3 and H6, F5=8.5 Hz, JH2, F5 and H6, F3=2Hz=22 Hz); 19F NMR δ −116.0 (d, 2F, F3+5, JF3, H2 and F5, 6=7.5 Hz); MS m/z 265 (M+Na+, 10), 243 (M+H+, 100), 211 (M-CH2OH, 85). Anal. (C11H12N2O2F2) C,H,N.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06852755B1uspto-grants-2005_02