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| | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Basic information |
| Product Name: | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER | | Synonyms: | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER;Methyl 3-Methyl-1H-pyrazole-4-carboxylate;Methyl 5-Methyl-1H-pyrazole-4-carboxylate;Methyl 3-Methylpyrazole-4-carboxylate;3-Cyclopentyl-1H-pyrazole-4-carboxylic acid methyl ester;1H-Pyrazole-4-carboxylic acid, 3-methyl-, methyl ester;Methyl 3-methyl-1H-pyrazol-4-carboxylate | | CAS: | 23170-45-8 | | MF: | C6H8N2O2 | | MW: | 140.14 | | EINECS: | | | Product Categories: | | | Mol File: | 23170-45-8.mol |  |
| | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Chemical Properties |
| Boiling point | 268.5±20.0 °C(Predicted) | | density | 1.217±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 12.15±0.50(Predicted) | | Appearance | Light yellow to yellow Solid |
| | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis |
| Uses | methyl 3-methyl-1h-pyrazole-4-carboxylate is used in the preparation of triazines and their phosphorus analogs via cyclization, ring transformation, aromatization, and substituent modification. | | Synthesis | General procedure for the synthesis of ethyl 3-methyl-1H-pyrazole-4-carboxylate from methanol and 3-methylpyrazole-4-carboxylic acid: 3-methylpyrazole-4-carboxylic acid (1.26 g, 10 mmol) was dissolved in methanol (100 mL) at 0 °C and thionyl chloride (5.73 g, 45 mmol) was added slowly, the reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was removed by vacuum evaporation. The residue was neutralized by adding saturated aqueous sodium bicarbonate solution and the mixture was extracted with ethyl acetate (100 mL x 3). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and the filtrate was concentrated in vacuum to give ethyl 3-methyl-1H-pyrazole-4-carboxylate (0.8 g, 57% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 7.87 (s, 1H), 3.84 (s, 3H), 2.53 (s, 3H). | | References | [1] Patent: WO2013/120104, 2013, A2. Location in patent: Paragraph 00183; 00184
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3644 - 3649
[3] Advanced Synthesis and Catalysis, 2010, vol. 352, # 11-12, p. 2041 - 2049 |
| | 5-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID METHYL ESTER Preparation Products And Raw materials |
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