ChemicalBook--->CAS DataBase List--->108130-10-5

108130-10-5

108130-10-5 Structure

108130-10-5 Structure
IdentificationBack Directory
[Name]

Ethyl 2,6-dichloro-4-Methylnicotinate
[CAS]

108130-10-5
[Synonyms]

Ethyl 2,6-dichloro-4-Methylnicotinate
[Molecular Formula]

C9H9Cl2NO2
[MDL Number]

MFCD21604262
[MOL File]

108130-10-5.mol
[Molecular Weight]

234.08
Chemical PropertiesBack Directory
[Boiling point ]

307.0±37.0 °C(Predicted)
[density ]

1.320±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

-3.68±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H402
[Precautionary statements ]

P501-P273-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Synthesis]

2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid

62774-90-7

Iodoethane

75-03-6

Ethyl 2,6-dichloro-4-Methylnicotinate

108130-10-5

2,6-Dichloro-4-methylpyridine-3-carboxylic acid (100 g, 485 mmol) and potassium carbonate (100 g, 728 mmol) were stirred in dimethylformamide (1.25 L) for 30 hours at room temperature. Subsequently, ethyl iodide (59.5 mL, 728 mmol) was added to the reaction system and stirring was continued for 18 hours. After completion of the reaction, water was added to the mixture and extracted with ethyl acetate (3×). The organic layers were combined, washed sequentially with water (2×) and brine (1×), dried over magnesium sulfate, and the solvent was evaporated to dryness under reduced pressure to afford ethyl 2,6-dichloro-4-methylpyridine-3-carboxylate (112 g), which was used for subsequent reactions without further purification.

[References]

[1] Patent: WO2013/156154, 2013, A1. Location in patent: Page/Page column 49
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