Sodium Hydroxide → HCID 18433637, compound
Reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[CH:8]=2)[S:4][C:3]=1[C:14]([O:16]C)=[O:15].[OH-].[Na+]>CO>[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[CH:8]=2)[S:4][C:3]=1[C:14]([OH:16])=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 3-amino-5-(3-chlorophenyl)-2-thiophenecarboxylate (1.0 g), 2M sodium hydroxide (2 mL) and methanol (10 mL) were heated at 70° C. for 2 days. The methanol was evaporated off and the residue was acidified with 2M hydrochloric acid. Extraction into ethyl acetate followed by drying (MgSO4) and evaporation of the solvent gave the sub-title acid (0.8 g).
Workup
- customThe methanol was evaporated off
- extractionExtraction into ethyl acetate
- customby drying
- custom(MgSO4) and evaporation of the solvent
Sources & evidence
- ORD record
- ord-ce36ed4f035149c6bd94f006df03f94a
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07358376B2
Reaction notes
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