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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 5-Methoxy-1,3-dimethyl-1H-pyrazole-4-carbaldehyde | HCID 2764304 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-methoxy-1,3-dimethyl-1H-pyrazole-4-carboxylic acid | HCID 23361779 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04226877 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-4953b2dab3c14992a046546aa51e786c |
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| Source note | uspto-grants-1980_10 |
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