Réaction #56596

ord-182c6791ac8b484092c777d8ef747440

Équation de réaction

Oc1cccc2ccccc12
1-naphtol
CN(C)c1ccc(N=Nc2ccc(N)cc2)c2ccccc12
1-(4-amino-phenylazo)-4-(dimethylamino)naphtalene
O=N[O-].[Na+]
sodium nitrite
CN(C)c1ccc(N=Nc2ccc(N=Nc3ccc(O)c4ccccc34)cc2)c2ccccc12
desired product
Rendement 74.2%
CN(C)c1ccc(N=Nc2ccc(N=Nc3ccc(O)c4ccccc34)cc2)c2ccccc12
1-[4-(4-(Dimethylamino)-naphthylazo)-phenylazo]-4-hydroxy-naphtalene
Rendement 74.2%

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction temperature below 4° C
  2. 2
    workup.ADDITIONAfter complete addition
  3. 3
    Autrethe reaction temperature below 5° C
  4. 4
    workup.ADDITIONAfter complete addition
  5. 5
    workup.STIRRINGthe reaction mixture was further stirred for 1 h at about 5° C.
  6. 6
    FiltrationThe resulting brownish precipitate was filtered off
  7. 7
    Lavagewashed with water (100 ml) and methanol (50 ml)
  8. 8
    AutreCrystallisation in methanol

Mode opératoire

2.9 g of 1-(4-amino-phenylazo)-4-(dimethylamino)naphtalene were dissolved in a mixture of 2.5 ml of HCl 37% and 5 ml of water. The obtained solution was cooled to 0° C., followed by dropwise addition of 0.69 g of sodium nitrite in 3 ml of water, while keeping the reaction temperature below 4° C. After complete addition, stirring was continued for 45 min at about 4° C. and the obtained mixture was then added to an ice-cooled solution of 1.44 g of 1-naphtol in NaOH/water (1.1 g/11 ml, while keeping the reaction temperature below 5° C. After complete addition, the reaction mixture was further stirred for 1 h at about 5° C. and then poured into 100 ml of water. The resulting brownish precipitate was filtered off, washed with water (100 ml) and methanol (50 ml). Crystallisation in methanol gave 3.3 g of the desired product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07419620B2uspto-grants-2008_09