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HRID 328025作成日:2026年10月26日

Chromone → 2-[6-[[3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl]oxy]hexyl]-6-[(6-methoxy-6-oxohexyl)oxy]benzenepropanoic Acid Methyl Ester

https://huagongshe.com/reaction/328025

反応式

関与物質

役割名称HCID仕込み量
反応物ChromoneHCID 10286—
反応物2-[(6-Methoxy-6-oxohexyl)oxy]-6-[6-[[4-oxo-8-(3-phenylpropyl)-4H-1-benzopyran-7-yl]oxy]hexyl]benzenepropanoic Acid Methyl EsterHCID 53867893—
触媒PalladiumHCID 23938—
溶媒Ethylacetate methanolHCID 21584119—
生成物2-[6-[[3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl]oxy]hexyl]-6-[(6-methoxy-6-oxohexyl)oxy]benzenepropanoic Acid Methyl EsterHCID 5419099338%

反応手順

A 1.0 g (1.49 mmol) sample of 2-[(6-methoxy-6-oxohexyl)oxy]-6-[6-[[4-oxo-8-(3-phenylpropyl)-4H-1-benzopyran-7-yl]oxy]hexyl]benzenepropanoic acid methyl ester from the preceding example was catalytically hydrogenate over 10% palladium on carbon, in 30 mL of 1:1 methanol-ethyl acetate, at room temperature and 1 atmosphere, using thin layer chromatography to monitor the reduction of the starting chromone. The catalyst was filtered and the filtrate was concentrated in vacuo giving an oily product which was purified by flash-chromatography. There was obtained 0.38 g (38%) of the title chromanone as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05273999
出典データセットuspto-grants-1993_12
ORD IDord-be1c3294c4da460286c65516666d2c21
出典メモuspto-grants-1993_12