Sodium Hydroxide → Laurolactam
Reaction equation
[C:1]1(=[O:14])[NH:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C1(C)C=CC=CC=1.[OH-].[Na+]>O>[C:1]1(=[O:14])[NH:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 85 °C
Procedure
50 g of water was added to 500 g of the laurolactam/toluene solution prepared by step C4 and the mixture was allowed to stand at 85° C. for 10 min and the phases were separated to obtain a light liquid phase. This operation was further repeated twice. To the light liquid phase obtained was added 64 g of a 1 mol/L aqueous sodium hydroxide solution, and the mixture was stirred at 85° C. for 10 min and then allowed to stand, followed by taking a light liquid phase (referred to as a post-treatment solution). The resulting light liquid phase was evaporated to remove toluene and then distilled (bottom temperature: 190° C., degree of vacuum: 3 to 4 torr, reflux ratio: 1, Sulzer packing: 7 plates) to give laurolactam.
Workup
- customthe phases were separated
- customto obtain a light liquid phase
- customTo the light liquid phase obtained
- customThe resulting light liquid phase was evaporated
- customto remove toluene
- distillationdistilled
- temperature(bottom temperature: 190° C., degree of vacuum: 3 to 4 torr, reflux ratio: 1, Sulzer packing: 7 plates)
Sources & evidence
- ORD record
- ord-f0ae29d81a894f5886ab11ae9ad369f0
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962826B2
Reaction notes
Loading…