HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378969Generated: November 2, 2026
Hydrochloric Acid → 3-(2-Methoxypyrimidin-5-yl)prop-2-enoic acid
https://huagongshe.com/reaction/1378969
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | methyl (E)-3-(2-methoxy-5-pyrimidinyl)acrylate | HCID 10774171 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-Methoxypyrimidin-5-yl)prop-2-enoic acid | HCID 10654948 | 95.9% |
Reaction Steps
To 1.26 g of methyl (E)-3-(2-methoxy-5-pyrimidinyl)acrylate were added 40 ml of methanol and 3.25 ml of a 4N potassium hydroxide aqueous solution, and the mixture was stirred at 50° C. for 2 hours. To the reaction mixture was added 0.5N hydrochloric acid, and the solution was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to give 1.12 g (6.22 mmol) of (E)-3-(2-methoxy-5-pyrimidinyl)acrylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05670492 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-e65df0f16b6d445db93dc84f11b0c931 |
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| Source note | uspto-grants-1997_09 |
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