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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50003Generated: October 25, 2026

Water → 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid

https://huagongshe.com/reaction/50003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactantethyl 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylateHCID 137485—
SolventMethanolHCID 887—
Product5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic AcidHCID 1107379293.5%

Reaction Conditions

Temperature8 °C

Reaction Steps

5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester (806 g), potassium hydroxide (548 g), water (2400 mL) and methanol (300 mL) were refluxed for two hours with stirring and then cooled to 8° C. The mixture was extracted twice with dichloromethane. The aqueous layer was adjusted to pH 4 with 1000 mL of 10 N hydrochloric acid keeping the temperature under 15° C. Water was added to facilitate stirring. The solid was collected by vacuum filtration, washed three times with water and dried under vacuum at 50° C. to give 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic (645 g, 93.5% yield) acid as a yellow solid. NMR (DMSO-d6) δ2.40, 2.43 (2×s, 2×3H, 2×CH3), 9.57 (s, 1H, CHO), 12.07 (br s, 2H, NH+COOH). MS m/z 168 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710067B2
Source datasetuspto-grants-2004_03
ORD IDord-f1deff7774114072976ffeda820bbfe9
Source noteuspto-grants-2004_03