Methanol → 5-Trifluoromethyl-pyridine-2-carboxylic acid methyl ester
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[CH:5][C:6]([C:9]([OH:11])=[O:10])=[N:7][CH:8]=1.S(Cl)(Cl)=O.[CH3:18]O>>[CH3:18][O:10][C:9]([C:6]1[CH:5]=[CH:4][C:3]([C:2]([F:12])([F:1])[F:13])=[CH:8][N:7]=1)=[O:11]Participants
4
Procedure
A solution of 5-(trifluoromethyl)-pyridine-2-carboxylic acid (CAN 80194-69-0, 3 g, 15.7 mmol) and sulfurous dichloride (0.1 mL) in methanol (30 mL) was stirred under reflux conditions overnight. Removal of the solvent provided the crude title compound which was purified by column chromatography (silica gel, 20 g, 10% ethyl acetate in petroleum ether) to obtain the title compound (2.7 g, 84%) as white solid; MS (EI): m/e=206.1 [M+H]+.
Workup
- customRemoval of the solvent
- customprovided the crude title compound which
- customwas purified by column chromatography (silica gel, 20 g, 10% ethyl acetate in petroleum ether)
Sources & evidence
- ORD record
- ord-54fae1011bab422a803ad12e717d7ac3
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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