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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349901Generated: October 29, 2026

[1-(3,5-Dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol → 1-(3,5-Dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehyde

https://huagongshe.com/reaction/349901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[1-(3,5-Dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanolHCID 23024986—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product1-(3,5-Dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehydeHCID 2302506897.5%

Reaction Steps

A mixture of [1-(3,5-dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol (23.8 g), activated manganese dioxide (50.00 g), and tetrahydrofuran (200 ml) was stirred at room temperature for two hours. After the manganese dioxide was removed by filtration, the filtrate was concentrated. The colorless crystals obtained were collected by filtration to yield 1-(3,5-dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehyde (23.10 g, yield: 97%). This was recrystallized from tetrahydrofuran-hexane. Melting point: 117–118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-6e398ebc86d647c29c5ca98b1aa5bc2d
Source noteuspto-grants-2007_02