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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221874Generated: October 26, 2026

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

https://huagongshe.com/reaction/2221874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazol-4-yl}methanolHCID 69216957—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazole-4-carbaldehydeHCID 8660581897%

Reaction Steps

A mixture of {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazol-4-yl}methanol (3.80 g), activated manganese dioxide (12.0 g) and tetrahydrofuran (150 mL) was stirred at room temperature for 15 hrs. Manganese dioxide was removed by filtration and the filtrate was concentrated. The obtained crystals were collected by filtration to give 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazole-4-carbaldehyde (3.64 g, yield 97%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 155-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-5fdb280c74fe4384aa29f500a747beef
Source noteuspto-grants-2008_05