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HRID 1093977作成日:2026年10月26日

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

https://huagongshe.com/reaction/1093977

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium ethoxideHCID 2723922—
反応物5-Trichloroacetyl-1H-pyrrole-3-carbaldehydeHCID 12459977—
生成物Ethyl 4-formyl-1H-pyrrole-2-carboxylateHCID 321486—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133889B2
出典データセットuspto-grants-2012_03
ORD IDord-189a90f457f5477792b9196a574b6d71
出典メモuspto-grants-2012_03