Reacción #3874

ord-c71b9f3cdcad49d1b3a53a42a03aed7c

Ecuación de reacción

Cl
hydrochloric acid
O.[Li][OH]
LiOH.H2O
Nc1cccc2c1OC(F)(F)O2
2,2-difluoro-4-amino-1,3-benzodioxole
O=[N+]([O-])c1cc([N+](=O)[O-])c(Cl)c(C(F)(F)F)c1
2,4-dinitro-6-trifluoromethylchlorobenzene
O=[N+]([O-])c1cc([N+](=O)[O-])c(Nc2cccc3c2OC(F)(F)O3)c(C(F)(F)F)c1
2,2-difluoro-4-[2',4'-dinitro-6'-(trifluoromethyl)anilino]-1,3-benzodioxole

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe resultant reaction mixture
  2. 2
    workup.STIRRINGis stirred at 0° C. for 20 minutes
  3. 3
    workup.WAITAfter 5 hours
  4. 4
    Extracciónextracted several times with diethyl ether
  5. 5
    LavadoThe combined ether phases are washed three times with a 5% solution of sodium carbonate
  6. 6
    Secadowith 5% hydrochloric acid and dried over sodium sulfate
  7. 7
    Otrothe solvent is evaporated off in vacuo
  8. 8
    Otroare recrystallised in toluene

Procedimiento

20.8 g of LiOH.H2O are added at 0° C. to a solution of 24.5 g of 2,2-difluoro-4-amino-1,3-benzodioxole in 70 ml of dimethyl sulfoxide. The mixture is then stirred for 20 minutes. Subsequently, a solution of 38.3 g of 2,4-dinitro-6-trifluoromethylchlorobenzene in 70 ml of dimethyl sulfoxide is added, and the resultant reaction mixture is stirred at 0° C. for 20 minutes and then heated to room temperature. After 5 hours, the mixture is poured into 350 ml of water, acidified with dilute hydrochloric acid and extracted several times with diethyl ether. The combined ether phases are washed three times with a 5% solution of sodium carbonate and then with 5% hydrochloric acid and dried over sodium sulfate, and the solvent is evaporated off in vacuo. The residue comprises 51.6 g of orange-brown crystals which are recrystallised in toluene. Yield: 41.6 g; melting point: 144°-146° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04722935uspto-grants-1988_02