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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414609Generated: October 30, 2026

1-Methyl-1H-pyrazole-4-carbaldehyde → 1-Methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/414609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-pyrazole-4-carbaldehydeHCID 573117—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product1-Methyl-1H-pyrazole-4-carboxylic acidHCID 64316052%

Reaction Steps

3.9 g of 1-methylpyrazole-4-aldehyde (described in J. Chem. Soc., page 3314, 1957) was dissolved in 20 ml of acetone, and while heating the solution, the Jones reagent was added. After the reaction, the excess of the Jones reagent was treated with a dilute aqueous alkaline solution, and the precipitate was collected by filtration. The filtrate was made weakly acidic and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give 2.3 g (yield 52%) of 1-methylpyrazole-4-carboxylic acid. m.p. 205°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792565
Source datasetuspto-grants-1988_12
ORD IDord-3a2c167913da47b9b99b181986edf847
Source noteuspto-grants-1988_12