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HRID 887043作成日:2026年10月25日

Acetic Acid → 4-(4-Hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl ester

https://huagongshe.com/reaction/887043

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrogen BromideHCID 260—
反応物4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 14866576—
溶媒EthanolHCID 702—
生成物4-(4-Hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 5965195245.7%

反応手順

A mixture of crude 4-(4-methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl ester (44 g, 175.8 mmol), acetic acid (300 mL) and 48% aqueous HBr (150 mL) was stirred at reflux for 10 h. The reaction was cooled to rt, concentrated at reduced pressure then partitioned between methylene chloride and water and the aqueous layer was extracted three times with methylene chloride and concentrated to provide a crude material. The crude material was dissolved in ethanol (125 mL) and added amberlyst then heated at 85° C. for 15 h. The reaction mixture was filtered over celite at rt and the filtrate was concentrated at reduced pressure and then partitioned between water and methylene chloride. The aqueous layer was extracted twice with methylene chloride to furnish a crude product and the crude product was purified by ISCO (330 g silica gel column) chromatography using 20 to 30% EtOAc in hexane to obtain a mixture (19 g) of 4-(4-hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl ester (MS m/z 235 (M−H) and p-hydroxypropiophenone. The mixture was used for the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08247414B2
出典データセットuspto-grants-2012_08
ORD IDord-5bd9a20672ff4b279b5517fed9502ad8
出典メモuspto-grants-2012_08