돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238397생성일: 2026년 10월 25일

Ethyl 4-methoxyphenylacetate → Ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/238397

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-methoxyphenylacetateHCID 84174—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물4-Cyano-2-methylbenzoyl chlorideHCID 86654215—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoateHCID 6717448888.7%

반응 단계

To a solution of (4-methoxy-phenyl)-acetic acid ethyl ester (25.96 g, 133.7 mmol) in anhydrous tetrahydrofuran (200 mL) was added lithium hexamethyldisilazide (200 mL, 1 M) at −78° C. under nitrogen. After being stirred for 15 min., a solution of A-5 (4-cyano-2-methylbenzoyl chloride) (24 g, 133.6 mmol) in anhydrous tetrahydrofuran (150 mL) was added dropwise, and the resulting mixture was stirred at room temperature overnight for 16 h. The reaction mixture was quenched by the addition of saturated aqueous ammonium chloride solution (200 mL), and the resultant mixture was extracted with ethyl acetate (100 mL×3). The combined organic layers were dried over anhydrous sodium sulfate (20 g), filtered, and evaporated. The residue was purified on silica gel column (petroleum ether/ethyl acetate=25:1) to give A-6 (ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate) (40 g, yield 88.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642628B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-c636269a56a941f6a2caef914f6df5ff
출처 메모uspto-grants-2014_02