Hydrogen Bromide → HCID 136134492, compound
Reaction equation
[Cl:1][C:2]1[C:3]([C:12]2[CH:17]=[CH:16][C:15]([O:18]C)=[CH:14][CH:13]=2)=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.Br>O>[Cl:1][C:2]1[C:3]([C:12]2[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=2)=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:9])[F:10])[CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 10.0 g (34.8 mmol) of 3-chloro-2-(4-methoxyphenyl)-5-trifluoromethylpyridine in 50 ml of 47% strength hydrobromic acid was heated at reflux temperatures for two hours. After cooling, the reaction mixture was diluted with 200 ml of water. After cooling for a few hours, the resulting crystals were separated off, washed with water and dried under reduced pressure. Yield: 8.0 g (84%) of colorless crystals.
Workup
- temperaturewas heated
- temperatureat reflux temperatures for two hours
- temperatureAfter cooling
- temperatureAfter cooling for a few hours
- customthe resulting crystals were separated off
- washwashed with water
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-b2c4a77541344300927b563253cb31d7
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06165941
Reaction notes
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