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HRID 1056作成日:2026年10月25日

6-(5-Methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanol → 6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofurancarbaldehyde

https://huagongshe.com/reaction/1056

反応式

関与物質

役割名称HCID仕込み量
反応物6-(5-Methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanolHCID 54094992—
触媒HCID 178418406HCID 178418406—
溶媒TetrahydrofuranHCID 8028—
生成物6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofurancarbaldehydeHCID 1969437269%

反応手順

A mixture of 6-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-methanol (21.0 g), activated manganese dioxide (52.0 g) and tetrahydrofuran (800 ml) was stirred at 60° to 65° C. for 6 hours. After the insoluble portion was filtered off, the filtrate was concentrated; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (2:98, v/v), crystals of 6-(5-methyl-2-phenyl-4-oxazolylmethoxy) benzofuran-2-carbaldehyde (14.3 g, 69%) were obtained, which was then recrystallized from dichloromethane-isopropyl propyl ether to yield colorless prisms having a melting point of 137° to 138° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723479
出典データセットuspto-grants-1998_03
ORD IDord-8d150316356a42dca5493597307eba01
出典メモuspto-grants-1998_03