Reacción #703986

ord-5f77568f7cc749cf891e9588f092aceb

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas collected on
  2. 2
    Filtracióna filter
  3. 3
    workup.ADDITIONthe filtrate was poured into 400 ml of methanol
  4. 4
    OtroThe isolated polymer was purified by two precipitations from tetrahydrofuran into methanol

Procedimiento

Copoly(N-vinyl carbazole-Vinyl alcohol) (II) (2.0 g) was dissolved in 50 ml of anhydrous pyridine. 3,5-Dinitrobenzoyl chloride (3.88 g) in 15 ml of anhydrous benzene was added with stirring to the pyridine solution. The resulting orange solution was stirred at room temperature for 4 hours. The small amount of solid remaining in the reaction mixture was collected on a filter and the filtrate was poured into 400 ml of methanol. The isolated polymer was purified by two precipitations from tetrahydrofuran into methanol to give 3.2 grams of a yellow powder. Nitrogen analysis demonstrated that the reaction of the alcohol groups with the acid chloride was nearly quantitative.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04076526uspto-grants-1978_02