Sodium Hydroxide → HCID 22268711, compound
Reaction equation
C[O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:7]=[C:6]([NH:14][CH2:15][CH3:16])[CH:5]=1.[OH-].[Na+]>C(O)C>[CH2:15]([NH:14][C:6]1[CH:5]=[C:4]([CH:9]=[C:8]([C:10]([F:11])([F:12])[F:13])[CH:7]=1)[C:3]([OH:17])=[O:2])[CH3:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
A mixture of 3-ethylamino-5-(trifluoromethyl)-benzoic acid methyl ester (1.38 g, 5.6 mmol), 5.5 mL 1M aqueous sodium hydroxide solution in 12 mL ethanol is shaken for 4 hours at 70° C. After cooling, the mixture is evaporated to dryness under reduced pressure. The resulting residue is dissolved in water, the pH adjusted to 5 with 1M hydrochloric acid. The precipitate is filtered off, washed with water and dried in vacuo to give the title compound.
Workup
- temperatureAfter cooling
- customthe mixture is evaporated to dryness under reduced pressure
- dissolutionThe resulting residue is dissolved in water
- filtrationThe precipitate is filtered off
- washwashed with water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-d90dd562c5374722bdd54607754eb441
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655669B2
Reaction notes
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