HRID377535

反应详情

EQUATION

反应方程式

HRID 377535 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

The thus obtained partially hydroxycarbonylmethylated polyhydroxystyrene, 90 g, was dissolved in 180 g of N,N-dimethylformamide. With stirring under ice cooling, 39.0 g of triethylamine and then 1.7 g of ethylene glycol di(1-chloroethyl) ether were added. Reaction was carried out for 30 minutes under ice cooling, 23.2 g of 1-chloroethyl ethyl ether was added, and reaction was carried out for a further 2 hours at room temperature. To this, 10.2 g of potassium carbonate and then 6.7 g of tert-butyl chloroacetate were added and reaction was carried out for 6 hours at 60° C. After the reaction mixture was allowed to cool down to room temperature, 500 g of ethyl acetate and 300 g of water were added thereto, followed by separation. The ethyl acetate layer was washed twice with 300 g of water and then concentrated in vacuum. The residue was dissolved in 300 g of methanol and added dropwise to 20 liters of water whereupon a powdery solid precipitated. The solid was collected by filtration, washed with 20 liters of water, and dried in vacuum at 40° C. for 24 hours. On 1H-NMR analysis, it was identified to be a polymer (Polym. 14) in which 24.0 mol % of the hydrogen atoms of hydroxyl groups in polyhydroxystyrene were replaced by 1-ethoxyethyl groups, 5.0 mol % were replaced by tert-butoxycarbonylmethyl groups, and the carboxyl group moieties which had been introduced in an amount of 2.0 mol % formed ester bonds with alcoholic hydroxyl groups of ethylene glycol di(1-hydroxyethyl) ether to provide crosslinking.

WORKUP

后处理

  1. customThe thus obtained partially hydroxycarbonylmethylated polyhydroxystyrene, 90 g
  2. customReaction
  3. customreaction
  4. waitwas carried out for a further 2 hours at room temperature
  5. customreaction
  6. waitwas carried out for 6 hours at 60° C
  7. customfollowed by separation
  8. washThe ethyl acetate layer was washed twice with 300 g of water
  9. concentrationconcentrated in vacuum
  10. dissolutionThe residue was dissolved in 300 g of methanol
  11. additionadded dropwise to 20 liters of water whereupon a powdery solid
  12. customprecipitated
  13. filtrationThe solid was collected by filtration
  14. washwashed with 20 liters of water
  15. customdried in vacuum at 40° C. for 24 hours
  16. additionthe carboxyl group moieties which had been introduced in an amount of 2.0 mol %