Sodium Hydroxide → HCID 86734791, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][CH:24]=1)[CH:6]=[CH:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH:17]([CH3:21])[C:18]([OH:20])=[O:19])=[O:9].[OH-].[Na+:26]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][CH:24]=1)[CH:6]=[CH:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH:17]([CH3:21])[C:18]([O-:20])=[O:19])=[O:9].[Na+:26]Participants
3
Procedure
162 Milligrams of 2-(3'-methoxycinnamoylamino)phenylpropionic acid were dissolved in an alcohol and an equivalent amount of sodium hydroxide was added to the solution. The mixture was warmed for 30 minutes and then concentrated under reduced pressure. The residue was taken up in a small amount of ethanol and ether was added to the ethanolic solution. The precipitated crystals were collected by filtration to obtain sodium 2-(3'-methoxycinnamoylamino)phenylpropionate.
Workup
- temperatureThe mixture was warmed for 30 minutes
- concentrationconcentrated under reduced pressure
- additionwas added to the ethanolic solution
- filtrationThe precipitated crystals were collected by filtration
Sources & evidence
- ORD record
- ord-4060da9058bd4930b89148b29e59f32e
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04026896
Reaction notes
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