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HRID 221849作成日:2026年10月24日

1-(4-Methoxyphenyl)butane-1,3-dione → 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/221849

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Methoxyphenyl)butane-1,3-dioneHCID 77640—
反応物Sodium ethoxideHCID 2723922—
反応物Ethyl chloro(hydroximino)acetateHCID 6816376—
溶媒EthanolHCID 702—
生成物4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl esterHCID 59652027—

反応手順

To 7.04 mL of 21% sodium ethoxide in ethanol (18.8 mmol) in 60 mL ethanol at 0° C. was added 4.70 g of 1-(4-methoxyphenyl)butane-1,3-dione (17.1 mmol) in 60 mL ethanol dropwise over 24 minutes. After 30 min a solution of 2.59 g of ethyl chloro-(hydroximino)acetate (17.1 mmol) in 30 mL ethanol was added dropwise over 6 minutes. The reaction was warmed to room temperature slowly. When TLC indicated the reaction was complete, the reaction was concentrated in vacuo. Water and saturated NaHCO3 was added and the product extracted with ethyl acetate. The ethyl acetate extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 8:1 hexane:ethyl acetate to give 4-(4-methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester which was dried overnight under high vacuum to give 3.74 g (71.8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207168B2
出典データセットuspto-grants-2012_06
ORD IDord-61dc1495a4384999961add7a19d8179b
出典メモuspto-grants-2012_06