반응 #831129

ord-edc7bd3e10fc4071b7d338ede1d4acd8

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타obtained in the same manner
  2. 2
    기타was reacted
  3. 3
    온도under reflux
  4. 4
    온도After cooling
  5. 5
    여과the precipitate was filtered off
  6. 6
    workup.ADDITIONthe filtrate was poured into H2O (1 l)
  7. 7
    기타was precipitated
  8. 8
    여과The precipitate was filtered
  9. 9
    세척washed with H2O
  10. 10
    기타dried under reduced pressure

실험 절차

A suspension of poly(p-hydroxystyrene) (4.0 g) obtained in the same manner as described in Reference Example 1, (2), tert-butyl monochloroacetate (3.0 g) and anhydrous K2CO3 (2.8 g) in acetone (35 ml) was reacted with stirring for 2 hours under reflux. After cooling, the precipitate was filtered off, the filtrate was poured into H2O (1 l) and was precipitated. The precipitate was filtered, washed with H2O and dried under reduced pressure to give 5.2 g of poly(tert-butyl p-vinylphenoxyacetate/p-hydroxystyrene) as white powder having Mw 11000 (GPC with polystyrene calibration). The polymer was found to have tert-butyl p-vinylphenoxyacetate unit and p-hydroxystyrene unit in a molar ratio of ca. 1:1 based on 1HNMR.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05558976uspto-grants-1996_09