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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246152Generated: October 26, 2026

Hydrochloric Acid → Ethyl 2,4-dimethyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/1246152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant2-Tert-butyl 4-ethyl 3,5-dimethyl-1h-pyrrole-2,4-dicarboxylateHCID 4347660—
SolventWaterHCID 962—
ProductEthyl 2,4-dimethyl-1H-pyrrole-3-carboxylateHCID 13748187.2%

Reaction Conditions

Temperature54 °C

Reaction Steps

3,5-Dimethyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester (2600 g) and ethanol (7800 mL) were stirred vigorously while 10 N hydrochloric acid (3650 mL) was slowly added. The temperature increased from 25° C. to 35° C. and gas evolution began. The mixture was warmed to 54° C. and stirred with further heating for one hour at which time the temperature was 67° C. The mixture was cooled to 5° C. and 32 L of ice and water were slowly added with stirring. The solid was collected by vacuum filtration and washed three times with water. The solid was air dried to constant weight to give of 2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester (1418 g, 87% yield) as a pinkish solid. 1H-NMR (dimethylsulfoxide-d6) δ 2.10, 2.35 (2×s, 2×3H, 2×CH3), 4.13 (q, 2H, CH2), 6.37 (s, 1H, CH), 10.85 (s, 1H, NH). MS m/z 167 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125905B2
Source datasetuspto-grants-2006_10
ORD IDord-8c7d8c19e6fa45a8a15c715dafd29231
Source noteuspto-grants-2006_10