Methanol → Methyl 2,5-Dichloronicotinate

HRID 221418Notes

Reaction equation

HRID 221418 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

5

Conditions

Temperature
0 °C

Procedure

A solution of 2,5-dichloronicotinic acid (20.2 g, 0.105 mol) 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 rt, and the reaction was allowed to stir for an additional 2 days at room temperature and the solvent was removed under reduced pressure to give an off-white residue. The residue was dissolved in Et2O (˜500 mL) and the resulting solution was washed successively with saturated aqueous NaHCO3 solution (˜300 mL), water (˜300 mL), and brine (˜300 mL). The organic layer was separated, dried over anhydrous MgSO4, and filtered. Removal of the solvent under reduced pressure yielded methyl 2,5-dichloronicotinate (21.0 g, 97%) as a white solid.

Workup

  1. customThe cooling bath was removed
  2. temperatureto warm to rt
  3. stirringto stir for an additional 2 days at room temperature
  4. customthe solvent was removed under reduced pressure
  5. customto give an off-white residue
  6. washthe resulting solution was washed successively with saturated aqueous NaHCO3 solution (˜300 mL), water (˜300 mL), and brine (˜300 mL)
  7. customThe organic layer was separated
  8. dry with materialdried over anhydrous MgSO4
  9. filtrationfiltered
  10. customRemoval of the solvent under reduced pressure

Sources & evidence

ORD record
ord-97402926099748f29bc5a2a5bb6c8cae
Source dataset
uspto-grants-2012_06
Patent number
US08207170B2

Reaction notes

Loading…