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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267303Generated: October 26, 2026

5-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedione → 5-[3-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedione

https://huagongshe.com/reaction/1267303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedioneHCID 57037009—
CatalystHCID 178418390HCID 178418390—
Solvent1,4-DioxaneHCID 31275—
Product5-[3-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedioneHCID 1587242996%

Reaction Steps

A mixture of 5-[4-[2-[5-methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedione (0.29 g), palladium-carbon (10%, 0.1 g) and dioxane (50 ml) was subjected to catalytic hydrogenation at room temperature under atmospheric pressure. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The concentrate was purified by means of a silica gel column chromatography. From the fractions eluted with chloroform-methanol (100:3) was obtained 5-[3-[4-[2-[5-methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedione (0.28 g, 96%). This product was recrystallized from dichloromethane-methanol to give colorless prisms, m.p.149-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552058B1
Source datasetuspto-grants-2003_04
ORD IDord-62785fad55c348eda698dd1cf279408e
Source noteuspto-grants-2003_04