HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850053Generated: November 2, 2026
Potassium Hydroxide → (2E)-3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoic acid
https://huagongshe.com/reaction/1850053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | methyl 3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoate | HCID 21936263 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2E)-3-(1-methyl-1H-pyrazol-4-yl)prop-2-enoic acid | HCID 1529858 | 72.5% |
Reaction Steps
(E)-methyl 3-(1-methyl-1H-pyrazol-4-yl)acrylate (0.24 g, 1.45 mmol) was dissolved in MeOH (10 mL). A 1M solution of KOH (5.8 mL) was added and the mixture was heated at 70° C. overnight. The reaction mixture was then evaporated under reduced pressure and water (10 mL) was added to the residue. This solution was carefully acidified to pH 4 with a 3M aqueous solution of HCl. The carboxylic acid precipitated and was extracted with ethyl acetate. The EtOAc layer was washed with water (2×10 mL) and brine (1×15 mL). It was dried over sodium sulfate, filtered and evaporated under vacuum to give (E)-3-(1-methyl-1H-pyrazol-4-yl)acrylic acid as a white solid (160 mg). ES+(M+H)+153
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957066B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-3665a68fb83a4f2da6c304c861425e85 |
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| Source note | uspto-grants-2015_02 |
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