Sodium Hydroxide → HCID 86734120, compound
Reaction equation
[CH2:1]([O:4][NH:5][C:6](=[C:9]1[C:14](=[O:15])[CH2:13][C:12]2([CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[CH2:11][C:10]1=[O:21])[CH2:7][CH3:8])[CH:2]=[CH2:3].[OH-:22].[Na+]>CC(C)=O.O>[CH2:1]([O:4][N:5]=[C:6]([C:9]1[C:14](=[O:15])[CH2:13][C:12]2([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]2)[CH2:11][C:10]=1[O:21][C:6](=[O:22])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:7][CH3:8])[CH:2]=[CH2:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 4-(1-allyloxyaminopropylidene)spirobicyclohexane-3,5-dione (1.5 g) in acetone (30 ml), sodium hydroxide (0.2 g) in water (1 ml) was added at room temperature and then benzoylochloride (0.7 g) was added. After stirring for 5 hr, the reaction mixture was poured into ice-water and extracted with chloroform. The extract was washed with one normal sodium hydroxide and dried over magnesium sulfate. The solvent was removed in vacuo and oily substance (0.8 g) was obtained.
Workup
- additionwas added
- extractionextracted with chloroform
- washThe extract was washed with one normal sodium hydroxide
- dry with materialdried over magnesium sulfate
- customThe solvent was removed in vacuo
- customoily substance (0.8 g) was obtained
Sources & evidence
- ORD record
- ord-958c953b86bc484b8876c0011bbb58eb
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03989737
Reaction notes
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