Sodium Hydroxide → HCID 23703556, compound

HRID 1816586Notes

Reaction equation

HRID 1816586 reaction equation
[Cl:1][C:2]1[CH:28]=[C:27]([Cl:29])[CH:26]=[CH:25][C:3]=1[C:4]([NH:6][CH2:7][C:8]1[CH:9]=[C:10]([CH2:16][CH:17]([O:21][CH:22]([CH3:24])[CH3:23])[C:18]([OH:20])=[O:19])[CH:11]=[CH:12][C:13]=1[O:14][CH3:15])=[O:5].[OH-].[Na+:31]>C(O)C>[Cl:1][C:2]1[CH:28]=[C:27]([Cl:29])[CH:26]=[CH:25][C:3]=1[C:4]([NH:6][CH2:7][C:8]1[CH:9]=[C:10]([CH2:16][CH:17]([O:21][CH:22]([CH3:24])[CH3:23])[C:18]([O-:20])=[O:19])[CH:11]=[CH:12][C:13]=1[O:14][CH3:15])=[O:5].[Na+:31]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 22493867HCID 22493867, compound

Product 1

HCID 23703556HCID 23703556, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

1.0 g of 3-(3-{[(2,4-dichlorobenzoyl)amino]methyl}-4-methoxyphenyl)-2-isopropoxypropanoic acid was dissolved in 5 ml ethanol, and 2.3 ml of 1 N aqueous sodium hydroxide solution was added thereto, and the solvent was removed, to give sodium 3-(3-{[(2,4-dichlorobenzoyl)amino]methyl}-4-methoxyphenyl)-2-isopropoxypropanoate was obtained.

Workup

  1. customthe solvent was removed

Sources & evidence

ORD record
ord-a5b254c004a44ae590d37b939f4582cd
Source dataset
uspto-grants-2005_04
Patent number
US06884821B1

Reaction notes

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