Réaction #2122473

ord-ac74c4a990b4403a9da01f052e483bcf

Équation de réaction

CN(C)c1ccc(C=O)cc1
4-dimethylaminobenzaldehyde
O=[N+]([O-])c1ccccc1
nitrobenzene
CN
methylamine
CN(C)c1ccc(C=C[N+](=O)[O-])cc1
red crystals
Rendement 41.1%
CN(C)c1ccc(C=C[N+](=O)[O-])cc1
1-(p-Dimethylaminophenyl)-2-nitroethylene
Rendement 41.1%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe dark red solid obtained
  2. 2
    Filtrationafter filtration
  3. 3
    Autrewas recrystallized from nitromethane
  4. 4
    Lavagerinsed with cold methanol

Mode opératoire

A mixture of 4-dimethylaminobenzaldehyde (1.5 g, 10 mmol) in 3 mL methanol, 0.61 g (10 mmol) nitrobenzene and 0.15 mL of 22% methylamine aqueous solution was stirred for 3 days. The dark red solid obtained after filtration was recrystallized from nitromethane and rinsed with cold methanol to yield 0.79 g (41.1%) of red crystals, mp 180.6-180.9° C. (ref mp 181° C. (see Richter-Egger, D. L. et al. J. Chem. Educ. 2001, 78, 1375-1378)). 1H NMR 3.08 (s, 6H, Ar—N(CH3)2); 6.68 (2H, d, JHH 8.7 Hz, Ar—H); 7.43 (2H, d, JHH 9.0 Hz, Ar—H); 7.50 (1H, d, JHH 13.2 Hz, Ar—CH); 7.97 (1H, d, JHH 13.5 Hz, CH—NO2).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08574453B2uspto-grants-2013_11