Acetic Acid → Btg H2O

HRID 611961

反応式

HRID 611961 の反応式
[OH:1]C1C=CC(C([C:11]2[CH:16]=[CH:15][C:14]([OH:17])=CC=2)(C)C)=CC=1.[CH2:18]1[O:20][CH2:19]1.[CH2:21]([CH:23]1[O:25][CH2:24]1)Cl.CN(C1C=CC(C(C2C=CC(N(C)C)=CC=2)=C2C=CC(=[N+](C)C)C=C2)=CC=1)C.[Cl-].[C:55](O)(=[O:57])C>[Br-].C([N+](CC)(CC)CC)C.C1(C)C=CC=CC=1>[CH3:11][CH2:16][CH2:15][CH2:14][O:17][CH2:21][CH2:23][O:25][CH2:24][CH2:18][O:20][CH2:19][CH2:55][OH:57].[OH2:1]

参加物

8

反応条件

温度
60 °C

実験手順

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 of f 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. after which 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.

後処理

  1. customTo a first 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
  2. additiona distillation head were added 1 part of DNP
  3. customTo a second 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
  4. temperatureBoth flasks were heated
  5. distillationto azeotropically distill of f the water
  6. customsparge
  7. concentrationAfter the water concentration in each flask
  8. additionSodium methoxide was added to each flask in an amount that OH
  9. temperatureHeat
  10. distillationto distill off
  11. customformed methanol
  12. distillationby distilling off half of the initial weight of toluene from the flask
  13. temperaturethe contents were refluxed for 1 hour with N2
  14. customsparge
  15. temperatureThe reaction mixture was then maintained at 70° C. until the alkalinity by titration
  16. additionThe contents of the first flask were added to the second flask, which
  17. distillationdistilled
  18. additionButoxytriglycol (BTG) and water were added

出典と根拠

ORDレコード
ord-70bd92c4ec4f4fa0ba18dc95290b399c
出典データセット
uspto-grants-1999_12
特許番号
US06002049

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