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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactantmethyl (E)-3-(2-methoxy-5-pyrimidinyl)acrylateHCID 10774171—
SolventMethanolHCID 887—
Product3-(2-Methoxypyrimidin-5-yl)prop-2-enoic acidHCID 1065494895.9%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670492
Source datasetuspto-grants-1997_09
ORD IDord-e65df0f16b6d445db93dc84f11b0c931
Source noteuspto-grants-1997_09