ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate

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CAS:139308-52-4
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Products Intro: Product Name:3-Bromo-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester
CAS:139308-52-4
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ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate Basic information
Product Name:ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate
Synonyms:ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate;3-Bromo-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester;1H-Pyrazole-4-carboxylic acid, 3-bromo-1-methyl-, ethyl ester;ethyl 3-bromo-1-methyl-pyrazole-4-carboxylate
CAS:139308-52-4
MF:C7H9BrN2O2
MW:233.06
EINECS:
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Mol File:139308-52-4.mol
ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate Structure
ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate Chemical Properties
Boiling point 290.7±20.0 °C(Predicted)
density 1.58±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-2.40±0.10(Predicted)
Safety Information
MSDS Information
ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate Usage And Synthesis
Synthesis
1-H-pyrazole-4-carboxylic acid,3-broMo,ethyl ester

1353100-91-0

Iodomethane

74-88-4

Ethyl 5-bromo-1-methyl-1H-pyrazole-4-carboxylate

105486-72-4

ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate

139308-52-4

To a solution of ethyl 3-bromopyrazole-4-carboxylate (5.6 g, 25.57 mmol) in DMF (200 ml) was added iodomethane (14.52 g, 102.28 mmol, 6.37 ml) and cesium carbonate (33.32 g, 102.28 mmol). The reaction mixture was stirred at 25°C for 12 hours. After completion of the reaction, the mixture was diluted with deionized water (1000 ml) and extracted with ethyl acetate (500 ml). The organic layer was subsequently washed with saturated brine (500 ml x 3), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was initially purified (4 g) by preparative HPLC (alkaline conditions). Further purification by silica gel column chromatography (eluent: petroleum ether/ethyl acetate = 10/1 to 5:1) afforded ethyl 5-bromo-1-methyl-1H-pyrazole-4-carboxylate (1 g, yield: 16.8%) and ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate (2 g, yield: 33.6%), both as white solid.

References[1] Patent: WO2018/64119, 2018, A1. Location in patent: Paragraph 0506; 0936
ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate Preparation Products And Raw materials
Raw materials1-H-pyrazole-4-carboxylic acid,3-broMo,ethyl ester-->Iodomethane-->N,N-Dimethylformamide-->Cesium carbonate
Tag:ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate(139308-52-4) Related Product Information
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