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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221726Generated: October 26, 2026

{1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazol-4-yl}methanol → 1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/2221726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazol-4-yl}methanolHCID 69216797—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazole-4-carbaldehydeHCID 8660576092.5%

Reaction Steps

A mixture of {1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazol-4-yl}methanol (0.38 g), activated manganese dioxide (1.20 g) and tetrahydrofuran (50 mL) was stirred at room temperature for 20 hrs. Manganese dioxide was removed by filtration, and the filtrate was concentrated. The obtained crystals were collected by filtration to give 1-benzyl-3-[(4{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}benzyl)oxy]-1H-pyrazole-4-carbaldehyde (0.35 g, yield 92%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 118-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-1979ea8c40c84d0282d700d802f4ead2
Source noteuspto-grants-2008_05