Reacción #43901
ord-7f60cc2eaa174291a37a3a0e14fbbd2f
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroA 3 L four-necked flask equipped with a stirrer
- 2OtroAfter the elapse of 40 min, it
- 3Temperaturathe mixture was cooled
- 4Otroseparated into two layers
- 5workup.DISTILLATIONThe thus separated organic layer was subjected to distillation treatment
Procedimiento
A 3 L four-necked flask equipped with a stirrer, a thermometer and a reflux condenser was charged with 1032 g (6.0 mol) of hydroxycitronellal, 520 g (6.4 mol) of a 37% by mass formaldehyde aqueous solution, 53 g (0.41 mol) of dibutyl amine and 10 g (0.09 mol) of hexanoic acid, and the contents in the flask were stirred while heating at 95° C. After the elapse of 40 min, it was confirmed that no hydroxycitronellal was present in the raw mixture, and then the mixture was cooled and separated into two layers. The thus separated organic layer was subjected to distillation treatment, thereby obtaining 1058 g (5.5 mol) of 3,7-dimethyl-2-methylene-7-hydroxyoctanal (purity as measured by gas chromatography: 95%) (yield based on theoretical amount: 92%).