Reacción #1943600

ord-7689c388765c4881b0b07f82f8a08e49

Ecuación de reacción

[H][H]
hydrogen
CC(C)(C)c1cc(N=Nc2ccccc2[N+](=O)[O-])c(O)c(C(C)(C)C)c1
2-nitro-2'-hydroxy-3',5'-di-tert-butylazobenzene
CO
methanol
[Na+].[OH-]
sodium hydroxide
CC(C)(C)c1cc(-n2nc3ccccc3n2)c(O)c(C(C)(C)C)c1
2-(2-Hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole
Rendimiento 85.8%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe catalyst was separated by filtration at 80° C
  2. 2
    Otrowas obtained in the usual manner in a yield of 85.8%

Procedimiento

Using the general procedure 6, 35.5 grams of 2-nitro-2'-hydroxy-3',5'-di-tert-butylazobenzene was suspended in 100 grams of tributyl phosphate, 50 grams of methanol and 4 grams of sodium hydroxide. To the suspension was then added 8 grams of Raney nickel catalyst and hydrogenation was carried out under 1 atmosphere of hydrogen at 45° C. for 7 hours. The catalyst was separated by filtration at 80° C. The above named product was obtained in the usual manner in a yield of 85.8%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04219480uspto-grants-1980_08