Réaction #531792
ord-817bc86595094b03b75420726869548e
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.WAITfollowed by 24-hour
- 2Températurerefluxing
- 3Autrethe reaction solution is moved into a separating funnel
- 4Autreseparation
- 5AutreAfter the organic phase was collected
- 6Autrethe desiccant agent was removed by filtration
- 7workup.DISTILLATIONthe solvent of the filtrate was distilled away under reduced pressure
- 8workup.DISSOLUTIONThe resultant solid was re-dissolved in 50 ml of toluene
- 9Lavagewas washed twice with 10 wt % of aqueous potassium hydroxide solution
- 10Lavagewas then washed with 50 ml of saturated saline
- 11AutreAfter that, the organic phase was collected
- 12AutreThe desiccant agent was removed by filtration
- 13workup.DISTILLATIONthe solvent of the filtrate was distilled away under reduced pressure
Mode opératoire
The 11-bromoundecan-1-ol 15 (3.68 g) and 4.88 g of p-cresol were dissolved in 20 ml of ethanol, and 2.57 g of potassium hydroxide was added to that, followed by 24-hour refluxing. After cooled to room temperature, the reaction solution is moved into a separating funnel, and 100 ml of ion-exchange water and 50 ml of methylene chloride were added so as to cause separation. After the organic phase was collected and was dehydrated with sodium sulfate, the desiccant agent was removed by filtration, and the solvent of the filtrate was distilled away under reduced pressure. The resultant solid was re-dissolved in 50 ml of toluene, and was washed twice with 10 wt % of aqueous potassium hydroxide solution, and was then washed with 50 ml of saturated saline. After that, the organic phase was collected, and was dehydrated with sodium sulfate. The desiccant agent was removed by filtration, and the solvent of the filtrate was distilled away under reduced pressure, to obtain 4.08 g of 11-(p-tolyloxy)undecan-1-ol 16, which is a white solid.