HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44257Generated: October 25, 2026
Ethanol → Ethyl 4-formyl-1H-pyrrole-2-carboxylate
https://huagongshe.com/reaction/44257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-Trichloroacetyl-1H-pyrrole-3-carbaldehyde | HCID 12459977 | — |
| Product | Ethyl 4-formyl-1H-pyrrole-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541412B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-3adbc94614604f3d9fa09f3bb4fa267c |
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| Source note | uspto-grants-2013_09 |
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