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HRID 413892作成日:2026年10月24日

p-Toluenesulfonic acid → 1-(3-Acetylphenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/413892

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物3'-AminoacetophenoneHCID 7417—
反応物Ethyl 2-acetyl-4-oxo-4-phenylbutanoateHCID 312893—
溶媒EthanolHCID 702—
生成物1-(3-Acetylphenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 10291357—

反応手順

3′-Aminoacetophenone (5 mmol, 0.7 g), 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid ethyl ester (5 mmol, 1.2 g), and tosic acid (0.1 g) were combined in ethanol, then heated under reflux. The resulting oil was purified over silica and yielded the named product as a solid (m.p. 102° C.-104° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06569890B2
出典データセットuspto-grants-2003_05
ORD IDord-e387fed91b954fe78ef985136441d255
出典メモuspto-grants-2003_05