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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221843생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/221843

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물4-PropanoylanisoleHCID 67144—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 14866576125.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207168B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-f7e3fa5d531c43d2a61a44b30b9655c7
출처 메모uspto-grants-2012_06