Reacción #1824308

ord-8f0973d921b74fde98f804f1e8baf2ee

Ecuación de reacción

[H][H]
hydrogen
CC1(C)OCC(COc2ccc([N+](=O)[O-])cc2[N+](=O)[O-])O1
4-(2,4-dinitrophenoxymethyl)-2,2-dimethyl-1,3-dioxolane
CC1(C)OCC(COc2ccc(N)cc2N)O1
4-(2,4-diaminophenoxymethyl)-2,2-dimethyl-1,3-dioxolane

Disolventes

Condiciones de reacción

Temperatura
5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONare dissolved
  2. 2
    OtroAfter the autoclave has been closed
  3. 3
    workup.ADDITION1.3 g of active carbon is added under nitrogen to the warm solution
  4. 4
    Filtraciónthe catalyst is filtered off
  5. 5
    workup.ADDITION42 g of 70% sulfuric acid are added dropwise to the solution
  6. 6
    OtroThe product precipitated
  7. 7
    Filtraciónis filtered off under suction
  8. 8
    Lavadowashed with methanol
  9. 9
    Otrodried

Procedimiento

215 ml of methanol are introduced into a 0.7 l autoclave, 85.3 g (0.3 mole) of 4-(2,4-dinitrophenoxymethyl)-2,2-dimethyl-1,3-dioxolane (step a) are dissolved therein and 0.6 g of palladium on active carbon 10% (Degussa) is added. After the autoclave has been closed and blanketed with nitrogen, hydrogenation is carried out under a pressure of 4 bar and at a temperature of 35 to 40° C. until no more hydrogen is taken up. 1.3 g of active carbon is added under nitrogen to the warm solution and the catalyst is filtered off. 42 g of 70% sulfuric acid are added dropwise to the solution while cooling with ice at 5° C. The product precipitated is filtered off under suction, washed with methanol and dried.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05961668uspto-grants-1999_10