Reacción #3874
ord-c71b9f3cdcad49d1b3a53a42a03aed7c
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otrothe resultant reaction mixture
- 2workup.STIRRINGis stirred at 0° C. for 20 minutes
- 3workup.WAITAfter 5 hours
- 4Extracciónextracted several times with diethyl ether
- 5LavadoThe combined ether phases are washed three times with a 5% solution of sodium carbonate
- 6Secadowith 5% hydrochloric acid and dried over sodium sulfate
- 7Otrothe solvent is evaporated off in vacuo
- 8Otroare 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.