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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233284Generated: October 26, 2026

2-Bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile → 3-[2-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile

https://huagongshe.com/reaction/233284

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrileHCID 10938527—
CatalystHCID 178418390HCID 178418390—
Solvent1,4-DioxaneHCID 31275—
Product3-[2-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrileHCID 1094758680.4%

Reaction Steps

A mixture of 2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (2.0 g), palladium-carbon (5%, 0.2 g) and dioxane (30 ml) was subjected to catalytic reduction under 1 atmospheric pressure at room temperature. The catalyst was filtered off, then the filtrate was concentrated under reduced pressure. The concentrate was subjected to a silica gel column chromatography. From the fractions eluted with ethyl acetate--hexane (2:3, v/v), was obtained 3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (1.3 g, 78%), which was recrystallized from ethyl acetate--hexane to give colorless crystals, m.p.105°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591862
Source datasetuspto-grants-1997_01
ORD IDord-9231ce2499c54fd2b6de30bc07e4dd0f
Source noteuspto-grants-1997_01