HCID 12993694, compound → 4,5,6-Trichloropyridine-2-carbaldehyde
Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[N:5]=[C:4]([CH2:10][OH:11])[CH:3]=1>ClCCl.[O-2].[Mn+4].[O-2]>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[N:5]=[C:4]([CH:10]=[O:11])[CH:3]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of (4,5,6-trichloropyridin-2-yl)methanol (3.83 g, 18 mmol) and manganese (IV) oxide (7.8 g, 90 mmol) in dichloromethane (50 mL) was stirred at room temperature for 24 hours. More manganese (IV) oxide (4 g, 46 mmol) was added and stirring was continued. After another 24 hours, the reaction mixture was suction filtered through a silica gel plug (10 g). After washing the silica gel plug with additional dichloromethane (2×25 mL), manganese (IV) oxide (8 g, 92 mmol) was added to the filtrate, and the mixture was stirred at room temperature for 72 hours. The reaction mixture was refiltered and the solvent was removed to provide 4,5,6-trichloropyridine-2-carbaldehyde (2.36 g, 11.4 mmol), mp 84-88° C.
Workup
- stirringstirring
- waitAfter another 24 hours
- filtrationfiltered through a silica gel plug (10 g)
- additionwas added to the filtrate
- stirringthe mixture was stirred at room temperature for 72 hours
- customthe solvent was removed
Sources & evidence
- ORD record
- ord-e480ce86ee5f4801906ac2dd295aa89c
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06784137B2
Reaction notes
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