1-Methyl-1H-1,2,4-triazole-5-carboxylic acid

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1-Methyl-1H-1,2,4-triazole-5-carboxylic acid Basic information
Product Name:1-Methyl-1H-1,2,4-triazole-5-carboxylic acid
Synonyms:1-Methyl-1H-1,2,4-triazole-5-carboxylic acid;2-Methyl-1,2,4-triazole-3-carboxylic acid;1H-1,2,4-Triazole-5-carboxylic acid, 1-methyl-;1-methyl-1H-1,2,4-triazole-5-carboxylic acid - [M87468]
CAS:815588-93-3
MF:C4H5N3O2
MW:127.1
EINECS:
Product Categories:
Mol File:815588-93-3.mol
1-Methyl-1H-1,2,4-triazole-5-carboxylic acid Structure
1-Methyl-1H-1,2,4-triazole-5-carboxylic acid Chemical Properties
Boiling point 369.5±25.0 °C(Predicted)
density 1.54±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka0.48±0.37(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
1-Methyl-1H-1,2,4-triazole-5-carboxylic acid Usage And Synthesis
Synthesis
1-METHYL-1,2,4-TRIAZOLE

6086-21-1

Carbon dioxide

124-38-9

1-Methyl-1H-1,2,4-triazole-5-carboxylic acid

815588-93-3

The general procedure for the synthesis of 1-methyl-1H-1,2,4-triazole-5-carboxylic acid from 1-methyl-1,2,4-triazole and carbon dioxide was as follows: to a stirred solution of 1-methyl-1,2,4-triazole (2.0 g, 24.0 mmol) in tetrahydrofuran (THF, 20 mL) was added slowly and dropwise at -78 °C n-butyllithium (19 mL, 12.0 mmol) and stirring was continued at this temperature for 2 hours. Subsequently, solid carbon dioxide (2 g) was added to the reaction system and stirred at -78 °C for 1 hour. The reaction mixture was gradually warmed to room temperature and stirring was continued for 16 hours. After confirming complete consumption of the feedstock by thin layer chromatography (TLC) monitoring, the reaction was quenched with deionized water (3 mL) and the resulting solid product was collected by filtration. The solid was purified by grinding with a solvent mixture of diethyl ether/n-pentane (10 mL/10 mL). Finally, the resulting white solid was dried under vacuum to afford the target compound 1-methyl-1H-1,2,4-triazole-5-carboxylic acid (Int-J, 2.0 g, 65.7% yield). The structure of the product was confirmed by 1H-NMR (500 MHz, DMSO-d6) and LCMS: 1H-NMR δ 7.70 (s, 1H), 4.01 (s, 3H); LCMS m/z: 128.3 [M+H]+.

References[1] Patent: WO2014/120800, 2014, A1. Location in patent: Paragraph 00161; page 65
[2] Patent: WO2009/147188, 2009, A1. Location in patent: Page/Page column 99
1-Methyl-1H-1,2,4-triazole-5-carboxylic acid Preparation Products And Raw materials
Raw materials1-Methyl-1,2,4-triazole-->Carbon dioxide-->n-Butyllithium-->Tetrahydrofuran
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