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HRID 221843作成日:2026年10月26日

Ethyl bromoacetate → 4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl ester

https://huagongshe.com/reaction/221843

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物4-PropanoylanisoleHCID 67144—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 14866576125.6%

反応手順

A solution of 4-methoxypropiophenone (24 g, 140 mmol) in tetrahydrofuran (220 mL) was cooled to 0° C. Lithium diisopropylamide, (2M solution in THF) (126 mL, 248 mmol) was added dropwise and warmed to rt for 30 min. The reaction was cooled again to 0° C. and ethyl bromoacetate (18 mL, 161 mmol) was added dropwise and warmed to rt for 30 min and then quenched with aqueous 1M HCl acid at 0° C. The aqueous layer was extracted twice with methylene chloride and the combined organics were washed with brine, dried (Na2SO4), filtered, and concentrated to give 4-(4-methoxyphenyl)-3-methyl-4-oxobutyric acid ethyl ester (44 g), MS m/z 205 (M−45).

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-f7e3fa5d531c43d2a61a44b30b9655c7
出典メモuspto-grants-2012_06