Reaktion #529786

ord-1ae50c228d1a4f6cb6067e5e0037d880

Reaktionsgleichung

Cl
hydrochloric acid
O
water
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
Di-t-butyl dicarbonate
C#Cc1ccc(O)cc1
poly(p-hydroxystyrene)
c1ccncc1
pyridine
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
p-hydroxystyrene p-(t-butyloxycarbonyloxy)styrene
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
p-hydroxystyrene p-(2-tetrahydropyranyloxy)styrene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA powdery matter thus precipitated
  2. 2
    Filtrationwas filtered off
  3. 3
    Waschenwashed with water
  4. 4
    Sonstigedried

Vorschrift

Di-t-butyl dicarbonate in an amount of 1.6 g was added to a solution containing poly(p-hydroxystyrene) [weight-average molecular weight: 11,000] in 40 ml of pyridine while stirring at room temperature. Therein, the reaction was run for 3 hours at room temperature, and the resultant solution was poured into a solution containing 20 g of conc. hydrochloric acid in 1 liter of ion-exchanged water. A powdery matter thus precipitated was filtered off, washed with water, and dried to give a p-hydroxystyrene/p-(t-butyloxycarbonyloxy)styrene (50/50) copolymer.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05891603uspto-grants-1999_04