Sodium Hydroxide → Azacycloundecan-2-one
Reaction equation
[C:1]1(=[O:11])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[N-:12]=[N+]=[N-].[Na+].[OH-].[Na+]>S(=O)(=O)(O)O.O>[C:1]1(=[O:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][NH:12]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 0 °C
Procedure
Cyclodecanone (n=6) (1.0 g) in 10 mL concentrated sulfuric acid was cooled to 0° C. and 0.54 g of sodium azide was added. The reaction continued to stir at 0° C. for 1 h and warmed to room temperature where it was stirred for two h. The solution was diluted with cold water and treated with cold 10% NaOH solution until pH=9. Extraction with ether (2×), drying over magnesium sulfate and evaporation of solvent provided 1.23 g of 2-azacycloundecanone.
Workup
- temperaturewarmed to room temperature where it
- stirringwas stirred for two h
- extractionExtraction with ether (2×)
- dry with materialdrying over magnesium sulfate and evaporation of solvent
Sources & evidence
- ORD record
- ord-b94c6932bf0b45b18cd81454ddf177d6
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07329683B2
Reaction notes
Loading…