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Meclofenamic Acid → Benzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl ester

HRID 1461424
Notes
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Reaction equation

HRID 1461424 reaction equation
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[NH:10][C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13]([OH:15])=[O:14].[C:20](Cl)(=O)C(Cl)=O>CO>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[NH:10][C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13]([O:15][CH3:20])=[O:14]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4037Meclofenamic AcidHCID 65578Oxalyl chloride

Product 1

HCID 76743Benzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl esterYield 89%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

2-[(2,6-Dichloro-3-methylphenyl)amino]benzoic acid is reacted with oxalyl chloride and methanol according to the procedure of Example 25 to give 2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid, methyl ester in 89% yield; mp 132°-134° C.

Sources & evidence

ORD record
ord-34e22260154f4ef1a84678d6820e26bd
Source dataset
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05075330

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes