Reaction #699142
ord-549af4d7de524fec8e65afb554566c1b
Reactants
Reagents
Conditions
Workup
- 1OtherTo a first 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
- 2workup.ADDITIONa distillation head were added 1 part of NP
- 3OtherTo a second 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube
- 4workup.ADDITIONa distillation head were added 1 part of NP
- 5TemperatureBoth flasks were heated
- 6workup.DISTILLATIONto azeotropically distill off the water
- 7Othersparge
- 8ConcentrationAfter the water concentration in each flask
- 9workup.ADDITIONSodium methoxide was added to each flask in an amount that OH
- 10TemperatureHeat
- 11workup.DISTILLATIONto distill off
- 12Otherformed methanol
- 13workup.DISTILLATIONby distilling off half of the initial weight of toluene from the flask
- 14TemperatureIn the first flask, the reaction mixture was then refluxed for 1 hour
- 15TemperatureThe reaction mixture was then maintained at 70° C. for about 2 hours
- 16Temperaturethe contents heated to 75-85° C. for 2 hours
- 17workup.ADDITIONwas added such that the mole ratio of Cl
- 18TemperatureThe reaction mixture was then refluxed until the alkalinity titration value
Procedure
To a first 250 ml round bottom flask equipped with a stirrer, nitrogen inlet tube, and a distillation head were added 1 part of NP--(EO)150 --OH (surfactant) 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 NP--(EO)50 --OH (surfactant) 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 55° 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. In the first flask, the reaction mixture was then refluxed for 1 hour. 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. for about 2 hours. When 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 and second flasks were mixed in a third flask such that the epoxy/alkoxide molar ratio was equal to 1:1 and the contents heated to 75-85° C. for 2 hours. When the epoxy titration value equaled zero, 1-chlorooctane was added such that the mole ratio of Cl:ONa was 1:1. The reaction mixture was then refluxed until the alkalinity titration value was zero. Butoxytriglycol (BTG) and water were added to give a clear yellow BTG/H2O/product ratio of 1:2:2 by weight.