Reaktion #2770

ord-5a412429988a4f6d803dc50ce52e1efd

Reaktionsgleichung

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
C1=COCCC1
3,4-dihydro-2H-pyran
O=S(=O)(O)O
sulfuric acid
C#Cc1ccc(O)cc1
Poly(p-hydroxystyrene)
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
p-tetrahydropyranyloxystyrene p-hydroxystyrene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe reaction solution was concentrated under reduced pressure
  2. 2
    SonstigeThe residue obtained
  3. 3
    Sonstigeto precipitate crystals
  4. 4
    FiltrationThe crystals were filtered off
  5. 5
    Waschenwashed with water
  6. 6
    Sonstigedried under reduced pressure

Vorschrift

Poly(p-hydroxystyrene) (weight average molecular weight: 9,600) in an amount of 9 g was dissolved in 100 ml of dimethoxyethane, and thereto 12.6 g of 3,4-dihydro-2H-pyran and 0.5 ml of sulfuric acid were added. This solution was stirred for 15 hours at 30°-40° C. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residue obtained was neutralized with sodium carbonate, and then poured into water to precipitate crystals. The crystals were filtered off, washed with water and dried under reduced pressure. Thus, 11.0 g of poly(p-tetrahydropyranyloxystyrene-p-hydroxystyrene) was obtained as white powder. The ratio of the p-tetrahydropyranyloxystyrene units to the p-hydroxystyrene units in the polymer obtained was determined to be 3:7 by 1H-NMR analysis.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731123uspto-grants-1998_03