Sodium Hydroxide → HCID 70259933, compound
Reaction equation
C([O:3][C:4](=[O:20])[C@H:5]([CH3:19])[N:6]([C:11]1[CH:16]=[CH:15][C:14]([S:17][CH3:18])=[CH:13][CH:12]=1)[CH2:7][CH2:8][CH2:9][CH3:10])C.[OH-].[Na+:22]>CO.O>[Na+:22].[CH3:18][S:17][C:14]1[CH:13]=[CH:12][C:11]([N:6]([CH2:7][CH2:8][CH2:9][CH3:10])[C@H:5]([C:4]([O-:20])=[O:3])[CH3:19])=[CH:16][CH:15]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
N-(4-Methylthiophenyl)-N-(n-butyl)alanine ethyl ester (3.0 g, 10.1 mmol) was dissolved in 50 mL methanol and 5 mL of water was added. Sodium hydroxide (0.41 g, 10.1 mmol) was dissolved in a minimum amount of water, and added to the aqueous methanol solution. The mixture was stirred 18 h at room temperature, and then the solvent was removed at reduced pressure. The resulting white solid was used without purification.
Workup
- customthe solvent was removed at reduced pressure
- customThe resulting white solid was used without purification
Sources & evidence
- ORD record
- ord-18c54a7989434ae3ba4c0b65e21fac06
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05747235
Reaction notes
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