ChemicalBook--->CAS DataBase List--->309740-49-6

309740-49-6

309740-49-6 Structure

309740-49-6 Structure
IdentificationBack Directory
[Name]

Methyl 1-Methyl-4-nitro-1H-pyrazole-5-carboxylate
[CAS]

309740-49-6
[Synonyms]

Methyl 1-Methyl-4-nitro-1...
Methyl 1-Methyl-4-nitropyrazole-5-carboxylate
Methyl 1-Methyl-4-nitro-1H-pyrazole-5-carboxylate
1H-Pyrazole-5-carboxylic acid, 1-methyl-4-nitro-, methyl ester
[Molecular Formula]

C6H7N3O4
[MDL Number]

MFCD02110822
[MOL File]

309740-49-6.mol
[Molecular Weight]

185.14
Chemical PropertiesBack Directory
[Melting point ]

38-41 °C(Solv: heptane (142-82-5))
[Boiling point ]

306.6±22.0 °C(Predicted)
[density ]

1.49±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-3.85±0.10(Predicted)
[Appearance]

Light brown to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 1-Methyl-4-nitro-1H-pyrazole-5-carboxylate(309740-49-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Pyrazole-3-carboxylic acid, 4-nitro-, methyl ester

138786-86-4

Iodomethane

74-88-4

Methyl 1-Methyl-4-nitro-1H-pyrazole-3-carboxylate

400877-57-8

Methyl 1-Methyl-4-nitro-1H-pyrazole-5-carboxylate

309740-49-6

The reaction was carried out with 4-nitro-1H-pyrazole-3-carboxylic acid methyl ester (2.0 g, 11.7 mmol) and iodomethane (2.0 g, 14.0 mmol) in the presence of potassium carbonate (1.62 g, 11.7 mmol) in acetone (60 mL) and stirred for 5 hours at 30°C. After completion of the reaction, the mixture was diluted with water and extracted with chloroform. The organic phases were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography (eluent: hexane-ethyl acetate from 4:1 to 1:1) to isolate two major products: methyl 1-methyl-4-nitro-1H-pyrazole-3-carboxylate (Rf values 0.43, 0.95 g, 44% yield) and methyl 1-methyl-4-nitro-1H-pyrazole-5-carboxylate (Rf values 0.71, 0.61 g, 28% yield).

[References]

[1] Patent: WO2011/154327, 2011, A1. Location in patent: Page/Page column 136; 137
[2] Patent: US2010/63106, 2010, A1. Location in patent: Page/Page column 11;13
[3] Patent: WO2008/51047, 2008, A1. Location in patent: Page/Page column 25; 28-29
[4] Patent: US2009/156582, 2009, A1. Location in patent: Page/Page column 30
[5] Patent: EP1847531, 2007, A1. Location in patent: Page/Page column 43
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