Sodium Hydroxide → HCID 69894550, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:33])[CH2:11][N:12]([CH2:19][C:20]1[CH:32]=[CH:31][C:23]([O:24][C:25]([CH3:30])([CH3:29])[C:26]([OH:28])=[O:27])=[CH:22][CH:21]=1)[CH2:13][C:14]1[O:15][CH:16]=[CH:17][CH:18]=1.[OH-].[Na+:35]>C(O)C>[Na+:35].[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:33])[CH2:11][N:12]([CH2:19][C:20]1[CH:21]=[CH:22][C:23]([O:24][C:25]([CH3:30])([CH3:29])[C:26]([O-:28])=[O:27])=[CH:31][CH:32]=1)[CH2:13][C:14]1[O:15][CH:16]=[CH:17][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.015 g (0.03 mmol) of the compound from Example 3-4 is dissolved in 0.5 ml of ethanol and treated with 0.3 ml of 1N aqueous sodium hydroxide solution. The reaction mixture is stirred for another 5 min and then concentrated using a rotary evaporator. The residue is taken up in a little toluene and the solvent is removed under reduced pressure. The product is then dried under reduced pressure for 20 hours. This gives 0.015 g (95.5% of theory) of the title compound.
Workup
- concentrationconcentrated
- customa rotary evaporator
- customthe solvent is removed under reduced pressure
- customThe product is then dried under reduced pressure for 20 hours
Sources & evidence
- ORD record
- ord-cc86c84946ec48dfab81ceeb57e9abbd
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06750236B2
Reaction notes
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