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1214337-05-9

1214337-05-9 Structure

1214337-05-9 Structure
IdentificationBack Directory
[Name]

Methyl 6-chloro-5-fluoropicolinate
[CAS]

1214337-05-9
[Synonyms]

Methyl 6-chloro-5-fluoropicolinate
methyl 6-chloro-5-fluoro-pyridine-2-carboxylate
Methyl 2-(6-(trifluoromethyl)pyridin-5-yl)acetate
6-Chloro-5-fluoro-pyridine-2-carboxylic acid methyl ester
2-Pyridinecarboxylic acid, 6-chloro-5-fluoro-, methyl ester
[Molecular Formula]

C7H5ClFNO2
[MDL Number]

MFCD14698137
[MOL File]

1214337-05-9.mol
[Molecular Weight]

189.57
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 6-chloro-5-fluoropicolinate(1214337-05-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Pyridinecarboxylic acid, 5-fluoro-, methyl ester, 1-oxide

1346555-30-3

Methyl 6-chloro-5-fluoropicolinate

1214337-05-9

Step 2: Synthesis of methyl 6-chloro-5-fluoropyridinecarboxylate 5-Fluoro-2-(methoxycarbonyl)pyridine-1-oxide (100 mg, 0.584 mmol) was dissolved in phosphorus trichloride (2 mL) and heated to reflux for 4 h under nitrogen protection. Upon completion of the reaction, the reaction solution was quenched by slow pouring into ice (15 g) and subsequently extracted with dichloromethane (30 mL × 2). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated. The resulting residue was purified by medium pressure liquid chromatography (MPLC) with 20% ethyl acetate/hexane as eluent to give 88 mg of white solid product in 79% yield.

[References]

[1] Patent: WO2011/139107, 2011, A2. Location in patent: Page/Page column 83
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