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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233814Generated: November 1, 2026

Hydrochloric Acid → Ethyl 5-ethyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/2233814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
Reactant2,2,2-trichloro-1-(5-ethyl-1H-pyrrol-2-yl)ethanoneHCID 10776454—
SolventDiethyl EtherHCID 3283—
ProductEthyl 5-ethyl-1H-pyrrole-2-carboxylateHCID 59748586%

Reaction Steps

Absolute EtOH (6 ml) was added to a 21 wt % solution of sodium ethoxide in EtOH (0.33 ml, 1.05 mmol) followed by the portion-wise addition of 2,2,2-trichloro-1-(5-ethyl-1H-pyrrol-2-yl)ethanone (J. Chem. Soc. Perkin Trans 1, 1996, 03) (2.1 g, 8.75 mmol) under nitrogen. The resulting yellow solution was stirred at room temperature for 30 minutes. Then the reaction was concentrated to give light orange oil. Hydrochloric acid (3 M, 2.5 ml) and diethyl ether (8 ml) were added to the oil and layers separated. The aqueous layer was extracted with diethyl ether (×2) and the combined organic extracts were washed with saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and concentrated to give the desired product as a white solid (1.27 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-b0f135ba785440128c71a3462093676e
Source noteuspto-grants-2010_05