Sodium Hydroxide → HCID 131711630, compound
Reaction equation
[OH:1][P:2]([CH2:11][C:12]([N:14]1[CH2:21][CH2:20][CH2:19][C@H:15]1[C:16]([OH:18])=[O:17])=[O:13])([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:3].[OH-].[Na+:23]>O>[Na+:23].[Na+:23].[OH:3][P:2]([CH2:11][C:12]([N:14]1[CH2:21][CH2:20][CH2:19][C@H:15]1[C:16]([O-:18])=[O:17])=[O:13])([CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:1].[OH:3][P:2]([CH2:11][C:12]([N:14]1[CH2:21][CH2:20][CH2:19][C@H:15]1[C:16]([O-:18])=[O:17])=[O:13])([CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-[[Hydroxy(phenylmethyl)phosphinyl]acetyl]-L-proline is dissolved in water and treated with two molar equivalents of aqueous sodium hydroxide. The resulting solution is lyophilized to give the product, 1-[[hydroxy(phenylmethyl) phosphinyl]acetyl]-L-proline disodium salt.
Sources & evidence
- ORD record
- ord-c87e90280fcd492d8818e7a3909c2c78
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04168267
Reaction notes
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