Sodium Carbonate → HCID 21249819, compound
Reaction equation
[Cl:1][C:2]1[C:3](C#N)=[N:4][C:5]([O:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:10]=2)=[CH:6][CH:7]=1.[C:21](=[O:24])([O-])[O-:22].[Na+].[Na+]>S(=O)(=O)(O)O>[Cl:1][C:2]1[C:3]([C:21]([OH:22])=[O:24])=[N:4][C:5]([O:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:17])([F:16])[F:18])[CH:10]=2)=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 120 °C
Procedure
3-chloro-2-cyano-6-[3-(trifluoromethyl)phenoxy] pyridine (2.58 g, 0.086 mol) was dissolved in 30 ml of 90% sulfuric acid. The obtained solution was heated and stirred at 120° C. for 1.5 hours. Thereafter, the obtained reaction solution was poured into ice water, and then treated with sodium carbonate to form a weakly-acidic solution, thereby precipitating solids. The precipitated solids were filtered out, washed with water and then dried.
Workup
- temperatureThe obtained solution was heated
- customThereafter, the obtained reaction solution
- customto form a weakly-acidic solution
- customprecipitating solids
- filtrationThe precipitated solids were filtered out
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-e760019b0e2c4e958ac12b3a9933ca03
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06159901
Reaction notes
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