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HRID 2221979作成日:2026年10月27日

[5-({4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]methanol → 5-({4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazole-4-carbaldehyde

https://huagongshe.com/reaction/2221979

反応式

関与物質

役割名称HCID仕込み量
反応物[5-({4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]methanolHCID 69214990—
触媒HCID 178418406HCID 178418406—
溶媒TetrahydrofuranHCID 8028—
生成物5-({4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazole-4-carbaldehydeHCID 8660579989.1%

反応手順

A mixture of [5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]methanol (3.10 g), activated manganese dioxide (10.0 g) and tetrahydrofuran (300 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 and washed with hexane to give 5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazole-4-carbaldehyde (2.75 g, yield 89%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 127-128° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07368578B2
出典データセットuspto-grants-2008_05
ORD IDord-f8dcec12ade7484c851e6e048eec7630
出典メモuspto-grants-2008_05