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HRID 351539作成日:2026年10月24日

Triethylamine → 1-(4-Methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dione

https://huagongshe.com/ja/reaction/351539

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl 4-FormylbenzoateHCID 15294—
反応物1-(4-n-Pentyloxyphenyl)acroleinHCID 22713222—
触媒3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chlorideHCID 2833352—
溶媒EthanolHCID 702—
生成物1-(4-Methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dioneHCID 2271322381.8%

反応手順

A suspension of 1-(4-n-pentyloxyphenyl)acrolein (2.38 g), methyl 4-formylbenzoate (1.97 g), 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride and triethylamine (0.91 ml) in ethanol (10 ml) was refluxed for 18 hours. After cooling, the solvents were removed under reduced pressure. The solids were taken up in 1N HCl and extracted with dichloromethane. The organic layer was washed successively with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated with diisopropyl ether, collected by filtration and dried under reduced pressure to give 1-(4-methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dione (3.41 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743776B2
出典データセットuspto-grants-2004_06
ORD IDord-1dfc266d3ef0430ca5d5774187bb1e33
出典メモuspto-grants-2004_06