Identification | More | [Name]
1-Phenyl-1H-pyrazole-4-carboxylic acid | [CAS]
1134-50-5 | [Synonyms]
1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID AKOS PAO-0321 ASINEX-REAG BAS 16289592 1-phenyl-pyrazole-4-carboxylicaci | [EINECS(EC#)]
413-030-8 | [Molecular Formula]
C10H8N2O2 | [MDL Number]
MFCD00514518 | [Molecular Weight]
188.18 | [MOL File]
1134-50-5.mol |
Hazard Information | Back Directory | [Synthesis]
Steps: Sodium hydroxide was dissolved in a 100 mL three-neck reaction flask containing 20 mL of water under nitrogen protection and magnetic stirring. Subsequently, 1-phenyl-1H-pyrazole-4-carbaldehyde was added in one go. Persistent insoluble products were observed even at temperatures of 45-50 °C. Hydrogen peroxide was added to the suspension in six portions over a period of 50 min. After the reaction lasted for 5 h at 50 °C, monitoring by TLC showed that most of the raw material remained. Next, 10 mL of 1N NaOH solution (containing 0.4 g NaOH) and 5 g aqueous hydrogen peroxide were added. After continued stirring at 50 °C for 1 h, the insoluble product completely disappeared and TLC monitoring confirmed that the starting material had been completely consumed (color developer: dinitrophenylhydrazine). The reaction mixture was cooled to room temperature and poured into 150 mL of ice/2N HCl mixture (2:1 volume ratio). After stirring for 30 min, the white precipitate formed was filtered through a Brinell's funnel and washed three times with water. The precipitate was dissolved in 250 mL of ethyl acetate, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to give 2.25 g of white solid product (yield: 96%). | [References]
[1] Inflammopharmacology, 2018, vol. 26, # 1, p. 217 - 226 [2] Patent: US2006/34786, 2006, A1. Location in patent: Page/Page column 62-63 [3] Chemical and Pharmaceutical Bulletin, 1980, vol. 28, # 4, p. 1265 - 1269 [4] Patent: US2009/239810, 2009, A1. Location in patent: Page/Page column 72 |
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