Reacción #904

ord-9750ebabdd9f4e72aa5a98408ce4247f

Ecuación de reacción

N
ammonia
O
water
COC(=O)c1c(S(=O)(=O)Cl)ccc([N+](=O)[O-])c1C
2-methoxycarbonyl-3-methyl-4-nitrobenzenesulfonyl chloride
Cc1c([N+](=O)[O-])ccc2c1C(=O)NS2(=O)=O
4-Methyl-5-nitrosaccharin

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthe mixture is concentrated on a rotary evaporator
  2. 2
    Otroto remove water and THF
  3. 3
    workup.STIRRINGThe residue which remains is stirred with ethyl acetate
  4. 4
    Filtraciónfiltered off with suction
  5. 5
    Lavadowashed with ethyl acetate
  6. 6
    OtroAfter drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.)
  7. 7
    Otroare obtained

Procedimiento

104 ml of 25% ammonia solution are initially taken, 100 ml of water are added and a solution of 48.7 g (0.166 mol) of 2-methoxycarbonyl-3-methyl-4-nitrobenzenesulfonyl chloride in 70 ml of tetrahydrofuran is then added dropwise at 10° C. After stirring at 25° C. for three hours, the mixture is concentrated on a rotary evaporator to remove water and THF. The residue which remains is stirred with ethyl acetate, filtered off with suction and washed with ethyl acetate. After drying under reduced pressure, 34 g (0.131 mol)=79% of theory of a white solid of m.p.: 312° C. (dec.) are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723415uspto-grants-1998_03