2,5-Dichloro-3-nitropyridine → 5-Chloro-2-methoxy-3-nitropyridine
Reaction equation
[CH3:1][O-:2].[Na+].Cl[C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:8]([Cl:14])=[CH:7][N:6]=1>CO.O>[Cl:14][C:8]1[CH:9]=[C:10]([N+:11]([O-:13])=[O:12])[C:5]([O:2][CH3:1])=[N:6][CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of sodium methoxide (0.84 g, 16.6 mmol) in methanol (4 mL) was added dropwise to a solution of 2,5-dichloro-3-nitropyridine (1.00 g, 5.2 mmol) in methanol (10 mL) and the mixture was stirred and heated to reflux. After 7 hours, the mixture was cooled and diluted with water and the precipitate was filtered and washed with water to give the title compound (0.95 g, 97%) as a white solid.
Workup
- temperatureheated to reflux
- temperaturethe mixture was cooled
- filtrationthe precipitate was filtered
- washwashed with water
Sources & evidence
- ORD record
- ord-6c642c45855f4dfa9d1e10821150d8ec
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133200B2
Reaction notes
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