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

Participants

Reaction Steps

A mixture of {1-benzyl-3-([4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)benzyl]oxy)-1H-pyrazol-4-yl}methanol (0.80 g), activated manganese dioxide (2.50 g) and tetrahydrofuran (50 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 1-benzyl-3-([4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)benzyl]oxy)-1H-pyrazole-4-carbaldehyde (0.70 g, yield 89%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 141-142° C.

Provenance & Evidence