ChemicalBook--->CAS DataBase List--->815588-93-3

815588-93-3

815588-93-3 Structure

815588-93-3 Structure
IdentificationBack Directory
[Name]

1-Methyl-1H-1,2,4-triazole-5-carboxylic acid
[CAS]

815588-93-3
[Synonyms]

2-Methyl-1,2,4-triazole-3-carboxylic acid
1-Methyl-1H-1,2,4-triazole-5-carboxylic acid
1H-1,2,4-Triazole-5-carboxylic acid, 1-methyl-
[Molecular Formula]

C4H5N3O2
[MDL Number]

MFCD11100092
[MOL File]

815588-93-3.mol
[Molecular Weight]

127.1
Chemical PropertiesBack Directory
[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
[pka]

0.48±0.37(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

1-Methyl-1H-1,2,4-triazole-5-carboxylic acid(815588-93-3)1HNMR
Hazard InformationBack Directory
[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
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