Reaktion #93231

ord-8f382b6590454ba2819c2a33f9930e23

Reaktionsgleichung

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

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with 1N hydrochloric acid and water
  2. 2
    TrocknenThe methylene chloride solution of the product was dried with sodium sulfate
  3. 3
    Sonstigeevaporated
  4. 4
    SonstigeA polymerization grade sample was obtained by recrystallization from methanol

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04611061uspto-grants-1986_09