Réaction #985259

ord-f1ce2604a94c48c28b98acd16002239d

Équation de réaction

COc1ccc(C(=O)Nc2ccc([N+](=O)[O-])cc2)cc1
4-methoxy-4′-nitrothiobenzaniline
COc1ccc(C(=O)Nc2ccc([N+](=O)[O-])cc2)cc1
4-Methoxy-4′-nitrobenzanilide
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawesson's reagent
COc1ccc(C(=S)Nc2ccc([N+](=O)[O-])cc2)cc1
product 4
Rendement 129.3%
COc1ccc(C(=S)Nc2ccc([N+](=O)[O-])cc2)cc1
4-Methoxy-4′-nitrothiobenzanilide
Rendement 129.3%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    Températureto reflux for 4 hrs
  3. 3
    AutreThe solvent was evaporated
  4. 4
    Autrethe residue was purified
  5. 5
    Autrewith flush column (hexane:ethyl acetate=4:1)

Mode opératoire

A mixture of 4-methoxy-4′-nitrothiobenzaniline 3 (1.0 g, 3.7 mmol) and Lawesson's reagent (0.89 g, 2.2 mmol, 0.6 equiv.) in chlorobenzene (15 mL) was heated to reflux for 4 hrs. The solvent was evaporated and the residue was purified with flush column (hexane:ethyl acetate=4:1) to give 820 mg (77.4%) of the product 4 as orange color solid. 1HNMR(300 MHz, DMSO-d6) δ: 8.29(d, 2H, H-3′,5′), 8.00(d, J=8.5 Hz, 2H, H-2′,6′), 7.76(d, 2H), 7.03(d, J=8.4 Hz, 2H), 3.808.37(d, J=5.5 Hz, 2H, H-3′,5′), 8.17(d, J=6.3 Hz, 2H, H-2′, 6′), 7.48(d, J=6.6 Hz, 2H), 6.97(d, J=6.5 Hz, 2H), 3.75(s, 3H, MeO). (s, 3H, MeO).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07351401B2uspto-grants-2008_04