Reacción #50939

ord-08f8001d29c14f0b8f97fb256f161cd1

Ecuación de reacción

Cl
HCl
Nc1ccccc1S
2-aminothiophenol
CCOC(=O)C(=O)OCC
diethyl oxalate
O
water
CCOC(=O)c1nc2ccccc2s1
ethyl 2-benzothiazolecarboxylate
Rendimiento 36.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 4 hr
  2. 2
    workup.ADDITIONpoured into a solution
  3. 3
    workup.DISSOLUTIONthe oil dissolved
  4. 4
    Otroa solid formed
  5. 5
    TemperaturaThe solution is cooled in an ice bath
  6. 6
    Filtraciónthe solid is collected by vacuum filtration
  7. 7
    Lavadothe solids are washed with a solution
  8. 8
    Otroto afford a dark solid
  9. 9
    OtroThis material is purified by crystallization from hot (68° C.) ligroin

Procedimiento

A solution of 2-aminothiophenol (10.7 mL, 0.1 mol) in diethyl oxalate (27.3 mL, 0.2 mol) is heated at reflux for 4 hr. The solution is cooled to rt and poured into a solution consisting of water (150 mL), conc. HCl (50 mL) and 95% EtOH (70 mL). With stirring, the oil dissolved and a solid formed. The solution is cooled in an ice bath, the solid is collected by vacuum filtration and the solids are washed with a solution consisting of EtOH/water (25/75) to afford a dark solid. This material is purified by crystallization from hot (68° C.) ligroin to yield ethyl 2-benzothiazolecarboxylate (7.5 g, 36%): Elemental analysis for C10H9NO2S: Calc: C, 57.95; H, 4.38; N, 6.76. Found: C, 57.99; H, 4.28; N, 6.78.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06849620B2uspto-grants-2005_02