Reacción #1094

ord-e6119d1ed5fd4cad8ff5deeb55d6be7b

Ecuación de reacción

O=CO
formic acid
CC(=O)OC(C)=O
acetic anhydride
COC(=O)c1ccc(N)cc1S(=O)(=O)NC(C)(C)C
N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide
COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture is subsequently heated at 50°-60° C. for 2 h
  2. 2
    OtroThe cooling bath is removed
  3. 3
    workup.STIRRINGThe reaction mixture is then shaken up in 800 ml of ethyl acetate
  4. 4
    Lavadowashed with three times 150 ml of water
  5. 5
    SecadoThe organic phase is dried over magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent is distilled off
  7. 7
    Otrothe residue is recrystallized from ethyl acetate/n-heptane

Procedimiento

6.5 ml of formic acid are carefully added at 0° C. to 13 ml of acetic anhydride. The mixture is subsequently heated at 50°-60° C. for 2 h. A solution of 16.0 g (0.056 mol) of N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide in 50 ml of DMF is then added dropwise at 0° C. The cooling bath is removed and the mixture is stirred for a further 4 h at room temperature. The reaction mixture is then shaken up in 800 ml of ethyl acetate and washed with three times 150 ml of water. The organic phase is dried over magnesium sulfate, the solvent is distilled off, and the residue is recrystallized from ethyl acetate/n-heptane. The product is N-tert-butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide (14.23 g, 82% of theory) which melts at 113°-114° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723409uspto-grants-1998_03