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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903152Generated: October 31, 2026

Water → 5-methoxy-1,3-dimethyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/903152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium PermanganateHCID 516875—
Reactant5-Methoxy-1,3-dimethyl-1H-pyrazole-4-carbaldehydeHCID 2764304—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
Product5-methoxy-1,3-dimethyl-1H-pyrazole-4-carboxylic acidHCID 2336177958%

Reaction Steps

2.5 g (0.0162 mole) of 1,3-dimethyl-5-methoxy-4-pyrazole carboxaldehyde (prepared as described in Khim. Farm. Zh, 4, 19 (1970) [CA, 73, 3844 w, (1970)] was dissolved in a solution containing 50 ml of water, 2 ml of acetic acid and 0.6 ml of acetone. 2.56 g (0.0162 mole) of potassium permanganate was added in several portions. The reaction was stirred for 3 hours before decomposing the excess potassium permanganate with 3 ml of methanol and then made alkaline with ammonium hydroxide, heated on the steam bath for 1/2 hour, and filtered. The filtrate was evaporated to approximately 30 ml of solution which was then acidified to pH4 with concentrated HCl. The solid was then collected. 1.6 g (58% yield) was obtained, m.p. 179°-180° C., white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04226877
Source datasetuspto-grants-1980_10
ORD IDord-4953b2dab3c14992a046546aa51e786c
Source noteuspto-grants-1980_10