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HRID 977243作成日:2026年10月25日

4-[3-[4-[2-(1,3-Dioxolan-2-yl)ethyl]phenyl]-3-oxopropyl]-5-methyl-2-phenyloxazole → 3-[4-[3-(5-Methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]propionaldehyde

https://huagongshe.com/reaction/977243

反応式

関与物質

役割名称HCID仕込み量
反応物4-[3-[4-[2-(1,3-Dioxolan-2-yl)ethyl]phenyl]-3-oxopropyl]-5-methyl-2-phenyloxazoleHCID 19965613—
溶媒Acetic acid--water (1/1)HCID 21899381—
生成物3-[4-[3-(5-Methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]propionaldehydeHCID 1996562778%

反応手順

A mixture of 4-[3-[4-[2-(1,3-dioxolan- 2-yl)ethyl]phenyl]-3-oxopropyl]-5-methyl-2-phenyloxazole (2.17 g) and 50% acetic acid-water (60 ml) was stirred at 75°-80° C. for 4 hours. The reaction mixture was concentrated under reduced pressure, neutralized with an aqueous solution of sodium hydrogen carbonate and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure; the residue was subjected to silica gel column chromatography. From the fraction eluted with ether-hexane (1:1), 3-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]propionaldehyde (1.5 g, 78%) was obtained, which was then recrystallized from ether-isopropyl ether to yield colorless needles having a melting point of 92°-93° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05614544
出典データセットuspto-grants-1997_03
ORD IDord-318fe7fc4c294e4ab8274bae61c6eb92
出典メモuspto-grants-1997_03