Reacción #93231

ord-8f382b6590454ba2819c2a33f9930e23

Ecuación de reacción

C=C(C)C(=O)Cl
Methacrylyl chloride
CCN(CC)CC
triethylamine
CC(C)(C)c1cc(CCCO)cc(-n2nc3ccc(Cl)cc3n2)c1O
2-(2'-hydroxy-5'-hydroxypropyl-3'-tert-butylphenyl)-5-chloro-2H-benzotriazole
CC=CC(=O)OCCCc1cc(-n2nc3ccc(Cl)cc3n2)c(O)c(C(C)(C)C)c1
2-(2'-Hydroxy-5'-methyacrylyloxypropyl-3'-tert-butylphenyl)-5-chloro-2H-benzotriazole

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with 1N hydrochloric acid and water
  2. 2
    SecadoThe methylene chloride solution of the product was dried with sodium sulfate
  3. 3
    Otroevaporated
  4. 4
    OtroA polymerization grade sample was obtained by recrystallization from methanol

Procedimiento

Methacrylyl chloride (5.9 ml) and triethylamine (8.5 ml) were added dropwise at -5° C. to a solution of 2-(2'-hydroxy-5'-hydroxypropyl-3'-tert-butylphenyl)-5-chloro-2H-benzotriazole (20 g) in 250 ml of methylene chloride. The reaction mixture was stirred at 0° C. overnight and then washed with 1N hydrochloric acid and water. The methylene chloride solution of the product was dried with sodium sulfate, passed through alumina column and evaporated. The crude yield of the product was 22 g (90%). A polymerization grade sample was obtained by recrystallization from methanol--methylene chloride mixture, m.p. 74.5°-76.5° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04611061uspto-grants-1986_09