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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2,2,2-trichloro-1-(5-ethyl-1H-pyrrol-2-yl)ethanone | HCID 10776454 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 5-ethyl-1H-pyrrole-2-carboxylate | HCID 597485 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709503B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-b0f135ba785440128c71a3462093676e |
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| Source note | uspto-grants-2010_05 |
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