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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349902Generated: October 29, 2026

Ethanol → Ethyl 3-[1-(3,5-dihydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate

https://huagongshe.com/reaction/349902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantethyl(E)-3-[1-(3,5-dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]propenoateHCID 69421654—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-[1-(3,5-dihydroxybenzyl)-4-phenyl-3-pyrrolyl]propionateHCID 2302486795%

Reaction Steps

A mixture of ethyl(E)-3-[1-(3,5-dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]propenoate (19.0 g), 5% palladium-carbon (40.0 g), ethanol (200 ml), and tetrahydrofuran (200 ml) was stirred for 4 hours at room temperature under a hydrogen atmosphere. After the palladium-carbon was removed by filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and ethyl 3-[1-(3,5-dihydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate (12.10 g, yield: 95%) was obtained as an oily substance from the fraction eluted with ethyl acetate-hexane (3:2, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-7af82cdbbfdc49c2b8c95ebac2cd2a4f
Source noteuspto-grants-2007_02