Reaktion #440865

Reaktionsgleichung

poly(p-hydroxystyrene)

propylene glycol monomethyl ether acetate

→

desired compound

Ausbeute 69.3%

p-[1-(2-Cyclohexylethoxy)ethoxy]styrene p-hydroxystyrene

Ausbeute 69.3%

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwith heating
2. 2
   workup.DISTILLATIONthe solution was subjected to dehydration by distillation under a reduce pressure
3. 3
   workup.ADDITIONTo the solution were added 0.35 g of pyridinium p-toluenesulfonate and 22.4 g of 2-cyclohexylethanol
4. 4
   workup.ADDITIONThen, 17.5 g of tert-butyl vinyl ether was gradually added to the solution
5. 5
   workup.ADDITIONTo the reaction mixture were added 0.28 g of triethylamine and 320 ml of ethyl acetate
6. 6
   Waschenthe mixture was washed three times with each 150 ml of distilled water
7. 7
   workup.DISTILLATIONThe solvent was distilled off
8. 8
   Einengento concentrate
9. 9
   workup.DISSOLUTIONthe resulting oily substance was dissolved in 100 ml of acetone
10. 10
    workup.ADDITIONthe solution was gradually poured into 2 liters of distilled water
11. 11
    FiltrationThe powder thus-deposited was collected by filtration
12. 12
    Sonstigedried

Vorschrift

In 320 g of propylene glycol monomethyl ether acetate (PGMEA) was dissolved 70 g of poly(p-hydroxystyrene) (VP-8000, manufactured by Nippon Soda Co., Ltd.) with heating and the solution was subjected to dehydration by distillation under a reduce pressure and cooled to 20° C. To the solution were added 0.35 g of pyridinium p-toluenesulfonate and 22.4 g of 2-cyclohexylethanol. Then, 17.5 g of tert-butyl vinyl ether was gradually added to the solution, followed by reacting at 20° C. for 5 hours. To the reaction mixture were added 0.28 g of triethylamine and 320 ml of ethyl acetate and the mixture was washed three times with each 150 ml of distilled water. The solvent was distilled off to concentrate, the resulting oily substance was dissolved in 100 ml of acetone and the solution was gradually poured into 2 liters of distilled water. The powder thus-deposited was collected by filtration and dried to obtain 54 g of the desired compound. The Mw of the resin was 12,000 and the molecular weight distribution (Mw/Mn) thereof was 1.1.

Quelle