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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349891Generated: October 30, 2026

[1-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]methanol → HCID 86760413, compound

https://huagongshe.com/reaction/349891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[1-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]methanolHCID 69427144—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
ProductHCID 86760413HCID 8676041372%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of [1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]methanol (3.98 g), activated manganese dioxide (8.00 g), and toluene (50 ml) was stirred at 80° C. for 10 hours. After the manganese dioxide was removed by filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-4-phenylpyrrole-3-carbaldehyde (2.85 g, yield: 72%) was obtained as colorless crystals from the fraction eluted with ethyl acetate-hexane (2:3, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 117–118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-17c75f5799d7467da2555bae63ca9c60
Source noteuspto-grants-2007_02