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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253056생성일: 2026년 10월 26일

Hydrochloric Acid → Ethyl 4-(4-chlorophenyl)-3-oxobutanoate

https://huagongshe.com/reaction/253056

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(4-Chlorophenyl)acetic acidHCID 15880—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Potassium ethyl malonateHCID 3446434—
반응물Magnesium ChlorideHCID 5360315—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물Ethyl 4-(4-chlorophenyl)-3-oxobutanoateHCID 1084766395.3%

반응 단계

To a solution of ethyl malonate potassium salt (39 g) in acetonitrile (100 mL) was added magnesium chloride (26 g) and triethylamine (48.6 g) and the mixture was stirred at room temperature for 2 hours (solution A). To a solution of 4-chlorophenylacetic acid (18.6 g) in acetonitrile (100 mL) was added carbonyldiimidazole (19.5 g) at room temperature and the mixture was stirred at the same temperature fro 1.5 hours. To the reaction mixture was added the solution A prepared above at room temperature and the mixture was stirred at the same temperature for 30 minutes and at 80° C. for 2 hours. After cooling the reaction mixture to room temperature, thereto was added 2N HCl solution (260 mL) and the mixture was stirred. The organic layer was washed with an aqueous sodium hydrogencarbonate solution and a brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=8/1 to 6/1) to obtain ethyl 4-(4-chlorophenyl)-3-oxobutyrate (25 g, yield: 95%) as a liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872006B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-9cc9e4f4a7c54777ae89f9116869f7ee
출처 메모uspto-grants-2011_01