HRID377534

反应详情

EQUATION

反应方程式

HRID 377534 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

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, 49.5 g of triethylamine and then 1.9 g of 1,4-butane diol di(1-chloroethyl) ether were added. Reaction was carried out for 30 minutes under ice cooling, 13.6 g of tert-butyl dicarbonate was added, and reaction was carried out for a further 2 hours at 40° C. After the reaction mixture was allowed to cool down, 23.2 g of 1-chloroethyl ethyl ether was added and reaction was carried out for 2 hours at room temperature. To the reaction mixture were added 500 g of ethyl acetate and 300 g of water, 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. 10) in which 24.0 mol % of the hydrogen atoms of hydroxyl groups in polyhydroxystyrene were replaced by 1-ethoxyethyl groups, 7.0 mol % were replaced by tert-butoxycarbonyl 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 1,4-butane diol 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 40° C
  5. temperatureto cool down
  6. customreaction
  7. waitwas carried out for 2 hours at room temperature
  8. customfollowed by separation
  9. washThe ethyl acetate layer was washed twice with 300 g of water
  10. concentrationconcentrated in vacuum
  11. dissolutionThe residue was dissolved in 300 g of methanol
  12. additionadded dropwise to 20 liters of water whereupon a powdery solid
  13. customprecipitated
  14. filtrationThe solid was collected by filtration
  15. washwashed with 20 liters of water
  16. customdried in vacuum at 40° C. for 24 hours
  17. additionthe carboxyl group moieties which had been introduced in an amount of 2.0 mol %