反应 #2632

ord-aa1345f1ddf34fbca738e90d0801abc6

反应方程式

CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
bis-phenol A
ClCC1CO1
epichlorohydrin
C1CO1
ethylene oxide
ClCC1CO1
epichlorohydrin
CC(=O)O
acetic acid
CC(=O)O
acetic acid
CN(C)c1ccc(C(=C2C=CC(=[N+](C)C)C=C2)c2ccc(N(C)C)cc2)cc1.[Cl-]
methyl violet
CCCCOCCOCCOCCO.O
BTG H2O

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他To a first 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
  2. 2
    其他To a second 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
  3. 3
    温度Both flasks were heated
  4. 4
    workup.DISTILLATIONto azeotropically distill off the water
  5. 5
    其他sparge
  6. 6
    浓缩After the water concentration in each flask
  7. 7
    workup.ADDITIONSodium methoxide was added to each flask in an amount that OH
  8. 8
    温度Heat
  9. 9
    workup.DISTILLATIONto distill off
  10. 10
    其他formed methanol
  11. 11
    workup.DISTILLATIONby distilling off half of the initial weight of toluene from the flask
  12. 12
    温度the contents were refluxed for 1 hour with N2
  13. 13
    其他sparge
  14. 14
    温度The reaction mixture was then maintained at 70° C. until the alkalinity by titration
  15. 15
    workup.ADDITIONThe contents of the first flask were added to the second flask, which
  16. 16
    workup.DISTILLATIONdistilled
  17. 17
    workup.ADDITIONButoxytriglycol (BTG) and water were added

实验过程

To a first 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube, and a distillation head were added 1 part of DNP-(EO)6 -OH and 2 parts of toluene. To a second 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube, and a distillation head were added 1 part of bis-phenol A ethoxylated with about 180 moles of ethylene oxide and 2 parts of toluene. Both flasks were heated to azeotropically distill off the water with stirring +N2 sparge. After the water concentration in each flask was less than 50 ppm the mixture was cooled to 60° C. Sodium methoxide was added to each flask in an amount that OH:NaOMe=1:1 based on the calculated hydroxyl value of surfactant. Heat was applied to distill off formed methanol by distilling off half of the initial weight of toluene from the flask then the contents were refluxed for 1 hour with N2 sparge. The flask was cooled to 60° C. afterwhich 1.1 moles of epichlorohydrin were added per mole sodium alkoxide. The reaction mixture was then maintained at 70° C. until the alkalinity by titration approached zero. The excess epichlorohydrin was vacuum stripped. A 4.0 gram aliquot of the reaction mixture +4 grams of tetraethylammonium bromide were dissolved in 50 ml of glacial acetic acid and the resulting solution titrated with a 0.1036 N HClO4 in glacial acetic acid solution to a methyl violet end point for the amount of epoxide (epoxy titration). The difference in the total alkalinity minus the HClO4 titration equals the amount of epoxide. The contents of the first flask were added to the second flask, which had been cooled to 110° C. in an amount such that the epoxy/alkoxide molar ratio was equal to 1:1. This mixture was held at 110° C. overnight. When the epoxy titration value equaled zero, the remaining toluene was vacuum distilled. Butoxytriglycol (BTG) and water were added to give a clear yellow BTG/H2O/product ratio of 1:5:3 by weight.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05728895uspto-grants-1998_03