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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241712Generated: October 25, 2026

Ethanol → Ethyl 4-formyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/241712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
Reactant5-Trichloroacetyl-1H-pyrrole-3-carbaldehydeHCID 12459977—
ProductEthyl 4-formyl-1H-pyrrole-2-carboxylateHCID 321486—

Reaction Steps

To a solution of the compound obtained in Step B (83.7 mmoles) in ethanol (200 ml) there is added, dropwise and over 20 minutes, a solution of sodium ethanolate (13.4 mmoles) in ethanol (45 ml) at ambient temperature. After stirring for 3 hours, the mixture is evaporated to dryness and then taken up in ethyl ether (200 ml). To that organic phase there is added aqueous 2N HCl solution (150 ml) and the resulting mixture is stirred; the phases are then separated and the aqueous phase is extracted with ethyl ether. The organic phase is washed with saturated aqueous NaHCO3 solution and with saturated aqueous NaCl solution, dried over sodium sulphate, filtered and evaporated to dryness to yield the title product (brown crystals), which is used directly in the next Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653073B2
Source datasetuspto-grants-2014_02
ORD IDord-d71042ca904f4fe58d17cbfaa562a909
Source noteuspto-grants-2014_02