Sodium Hydroxide → HCID 22003631, compound
Reaction equation
[Cl:1][C:2]1[S:3][C:4]([CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=2)=[C:5]([C:7]([O:9]C)=[O:8])[N:6]=1.[OH-].[Na+]>O1CCCC1.O>[Cl:1][C:2]1[S:3][C:4]([CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=2)=[C:5]([C:7]([OH:9])=[O:8])[N:6]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The product from step (ii) (3.46 g) was treated with sodium hydroxide (0.7 g) in tetrahydrofuran (15 ml) and water (15 m) at room temperature. After 3 h the mixture was partitioned between 2M HCl and ethyl acetate. The organic phase was collected, dried (MgSO4) and solvent evaporated under reduced pressure to leave a colourless solid.
Workup
- customAfter 3 h the mixture was partitioned between 2M HCl and ethyl acetate
- customThe organic phase was collected
- dry with materialdried (MgSO4) and solvent
- customevaporated under reduced pressure
- customto leave a colourless solid
Sources & evidence
- ORD record
- ord-1fe122ffc1ad43009bd4d4e2c052f5d7
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06218376B1
Reaction notes
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