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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1365705생성일: 2026년 10월 25일

Ethyl Acetate → (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester

https://huagongshe.com/reaction/1365705

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyranHCID 57762532—
반응물(S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762562—
촉매Tri-o-tolylphosphineHCID 80271—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl esterHCID 5776252979.2%

반응 조건

온도80 °C

반응 단계

Under an argon atmosphere, palladium acetate (295 mg) and tris(2-methylphenyl)phosphine (384 mg) were added to a suspension of (S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (7.60 g), tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyran (8.00 g) and potassium carbonate (5.21 g) in DMF (90 ml), and the resulting mixture was stirred at 80° C. for 2 hours. After cooling the reaction solution to room temperature, ethyl acetate was added thereto, and the resulting mixture was washed 3 times with water and once with saturated brine, followed by drying the organic layer over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=2/1→1/4). The obtained crudely purified product was further purified by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=4/1) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester (9.80 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893046B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-5642043d8ce14c0a8be345bbdfc6bc91
출처 메모uspto-grants-2011_02