Methanol → Methyl 2,5-Dichloronicotinate
Reaction equation
[Cl:1][C:2]1[N:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:16]O>CCOCC>[Cl:1][C:2]1[N:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([O:6][CH3:16])=[O:5]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A solution of 2,5-dichloronicotinic acid (20.2 g, 0.105 mol, Aldrich) in methanol (500 mL) was cooled to 0° C. and neat thionyl chloride (38 mL, 63 g, 0.525 mol) was added over ˜30 min. The reaction mixture was stirred at 0° C. for 1 hour. The cooling bath was removed, the reaction temperature was allowed to warm to room temperature, and the reaction was allowed to stir for an additional 2 days at room temperature. The solvent was removed under reduced pressure to give an off-white residue. The residue was dissolved in ether (˜500 mL) and the resulting solution was washed successively with saturated aqueous sodium bicarbonate solution (˜300 mL), water (˜300 mL), and brine (˜300 mL). The organic layer was separated, dried over anhydrous magnesium sulfate, and filtered. Removal of the solvent under reduced pressure yielded methyl 2,5-dichloronicotinate (21.0 g, 97% yield) as a white solid.
Workup
- customThe cooling bath was removed
- temperatureto warm to room temperature
- stirringto stir for an additional 2 days at room temperature
- customThe solvent was removed under reduced pressure
- customto give an off-white residue
- washthe resulting solution was washed successively with saturated aqueous sodium bicarbonate solution (˜300 mL), water (˜300 mL), and brine (˜300 mL)
- customThe organic layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- customRemoval of the solvent under reduced pressure
Sources & evidence
- ORD record
- ord-dd7c7dd0228e4ca79224f99f126b064d
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07566718B2
Reaction notes
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