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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474328생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/474328

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물5-Chloro-2-methylbenzoic acidHCID 82009—
반응물Potassium ethyl malonateHCID 3446434—
반응물Magnesium ChlorideHCID 5360315—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoateHCID 54012347118%

반응 단계

To a stirring solution of 5-chloro-2-methylbenzoic acid (4.85 g, 28.4 mmol) in tetrahydrofuran (30 mL) was added N,N-carbonyldiimidazole (4.87 g, 30.0 mmol, 1.06 equiv). After 30 minutes, the reaction mixture was added to a suspension of potassium ethyl malonate (11.61 g, 68.22 mmol, 2.40 equiv) and magnesium chloride (3.27 g, 34.3 mmol, 1.21 equiv) in tetrahydrofuran (50 mL). The resultant suspension was heated at 50° C. After hours, the reaction mixture was partitioned between ethyl acetate and water. The organic portion was dried over magnesium sulfate, filtered, and concentrated to provide 8.07 g (118%) of ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate which was used without purification. LCMS (ESI) m+H=241.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637526B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-6902af7ba6ec4cafb811af10766cae5d
출처 메모uspto-grants-2014_01