Reacción #465969

ord-b7278315d1144850911926697803a758

Ecuación de reacción

O=C([O-])O.[Na+]
sodium bicarbonate
O=S(=O)(O)O.O=S(=O)=O
oleum
COC(=O)c1c(Cl)ccc(Cl)[n+]1[O-]
Methyl 3,6-dichloropyridine-2-carboxylate N-oxide
O=[N+]([O-])O
HNO3
O=C(O)c1nc(Cl)cc([N+](=O)[O-])c1Cl
yellow solid
O=C(O)c1nc(Cl)cc([N+](=O)[O-])c1Cl
4-Nitro-3,6-dichloropyridine-2-carboxylic Acid

Condiciones de reacción

Temperatura
65°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was cooled in an ice/water bath and to it
  2. 2
    OtroThe cooled reaction mixture
  3. 3
    ExtracciónThe product was extracted with ethyl acetate (2×150 mL)
  4. 4
    Secadothe combined extracts were dried (MgSO4)
  5. 5
    Concentraciónconcentrated

Procedimiento

Methyl 3,6-dichloropyridine-2-carboxylate N-oxide (5.0 g, 22.52 mmol) was dissolved in a minimum amount of H2SO4. The mixture was cooled in an ice/water bath and to it was slowly added 30% oleum (9.6 mL) and fuming HNO3 (9.6 mL), gradually heated to 65° C. and stirred for 48 hr. The cooled reaction mixture was diluted with ethyl acetate (200 mL) and to it was carefully added saturated sodium bicarbonate. The product was extracted with ethyl acetate (2×150 mL) and the combined extracts were dried (MgSO4) and concentrated to give 0.10 g of a yellow solid; mp 192-193° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06297197B1uspto-grants-2001_10