반응 #93231

ord-8f382b6590454ba2819c2a33f9930e23

반응 방정식

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

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with 1N hydrochloric acid and water
  2. 2
    건조The methylene chloride solution of the product was dried with sodium sulfate
  3. 3
    기타evaporated
  4. 4
    기타A polymerization grade sample was obtained by recrystallization from methanol

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04611061uspto-grants-1986_09