Reacción #3850
ord-d50e6d173a8247479425da3781712173
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaheater, cooling coils, automatic temperature controller
- 2Otroa gaseous N2 purge of the reactor
- 3workup.ADDITIONis introduced
- 4Otroto remove both oxygen and water
- 5TemperaturaWith continued N2 purging its temperature of the neo acid/catalyst solution is gradually raised to 150° C
- 6Otrothe N2 purge
- 7Otrothe reactor vents are sealed
- 8workup.ADDITIONEthylene oxide is then slowly added to the reactor
- 9Temperaturato maintain a reactor pressure of about 30 psig
- 10workup.ADDITIONTotal reaction time, from the start of ethylene oxide addition
- 11workup.WAITis about 55 minutes
- 12Otroa gaseous nitrogen purge
- 13workup.ADDITIONis introduced
- 14Temperaturathe reaction product is cooled to room temperature
Procedimiento
To a one liter stainless steel autoclave, equipped with a mechanical stirrer, heater, cooling coils, automatic temperature controller, and a tared ethylene oxide cylinder, in a series of runs is added 500 grams neodecanoic acid and 2.0 g of the selected catalyst. The reactor is heated to approximately 100° C. and a gaseous N2 purge of the reactor is introduced to remove both oxygen and water. With continued N2 purging its temperature of the neo acid/catalyst solution is gradually raised to 150° C. Upon reaching temperature, the N2 purge is stopped and the reactor vents are sealed. Ethylene oxide is then slowly added to the reactor to maintain a reactor pressure of about 30 psig. The flow of ethylene oxide is then stopped. The reaction mixture is stirred for an additional 20 minutes, until the reactor pressure decreases to 15 psig. Total reaction time, from the start of ethylene oxide addition is about 55 minutes. The reactor is then vented, a gaseous nitrogen purge is introduced, and the reaction product is cooled to room temperature. The crude ethylene glycol mononeodecanoate product mixture thereby obtained was analyzed by gas chromatography. The data obtained are set forth in Table II below.