2,3,5,6-Tetrachloro-4-hydrazinylpyridine → 2,3,5,6-Tetrachloropyridine
Reaction equation
Cl[O-].[Na+].[Cl:4][C:5]1[C:10]([Cl:11])=[C:9](NN)[C:8]([Cl:14])=[C:7]([Cl:15])[N:6]=1>>[Cl:4][C:5]1[C:10]([Cl:11])=[CH:9][C:8]([Cl:14])=[C:7]([Cl:15])[N:6]=1Participants
3
Procedure
To a reaction vessel containing 200 milliliters (0.14 mole) of 5.25 percent sodium hypochlorite was added 10 grams (0.04 mole) of 2,3,5,6-tetrachloro-4-hydrazinopyridine. The mixture was heated at the boiling point for 1 hour, cooled and the solid which precipitated was recovered by filtration and dried. The 2,3,5,6-tetrachloropyridine was recovered in a yield of 7.0 grams (84 percent of theoretical) and the structure of the product was confirmed by infrared analysis and vapor phase chromatography.
Workup
- temperatureThe mixture was heated at the boiling point for 1 hour
- temperaturecooled
- customthe solid which precipitated
- filtrationwas recovered by filtration
- customdried
- customThe 2,3,5,6-tetrachloropyridine was recovered in a yield of 7.0 grams (84 percent of theoretical)
Sources & evidence
- ORD record
- ord-e4317ae60db247cfa30922d20c9454f5
- Source dataset
- uspto-grants-1978_11
- Patent number
- US04127575
Reaction notes
Loading…