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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012133Generated: October 29, 2026

1-(4-methoxy-benzyl)-4-nitro-1H-pyrazole-3-carboxylic acid ethyl ester → 1-[(4-Methoxyphenyl)methyl]-4-nitro-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/1012133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-methoxy-benzyl)-4-nitro-1H-pyrazole-3-carboxylic acid ethyl esterHCID 58875016—
SolventSodium hydroxide methanolHCID 23721981—
Product1-[(4-Methoxyphenyl)methyl]-4-nitro-1H-pyrazole-3-carboxylic acidHCID 6710601790.2%

Reaction Steps

A mixture of 1-(4-methoxy-benzyl)-4-nitro-1H-pyrazole-3-carboxylic acid ethyl ester (15.9 g, 52 mmol) in 2 M aqueous NaOH/MeOH (1:1, 400 ml) was stirred at ambient temperature for 14 h. Volatile materials were removed in vacuo, the residue dissolved in EtOAc (200 ml), water (100 ml) added and the mixture taken to pH 3 using 1M aqueous HCl. The layers were separated and the organic portion washed with saturated aqueous sodium hydrogen carbonate. EtOAc was added to the aqueous layer which was acidified to pH 3-4, and the combined organic portions dried (MgSO4) and reduced in vacuo to give 1-(4-methoxy-benzyl)-4-nitro-1H-pyrazole-3-carboxylic acid (13 g, 86%) as a white solid. (LC/MS: Rt 2.63, [M+H]+ 292).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-a983167810b54e16bef919c6d424333d
Source noteuspto-grants-2011_07