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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752094생성일: 2026년 10월 24일

Barium hydroxide, octahydrate → (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid

https://huagongshe.com/ko/reaction/1752094

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참여 물질

역할이름HCID투입량
반응물Barium hydroxide, octahydrateHCID 17749109—
반응물(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl esterHCID 57762529—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acidHCID 1153340664.6%

반응 조건

온도0 °C

반응 단계

In a mixed solvent of THF (250 ml) and water (125 ml), (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester (9.80 g) was dissolved, and the resulting mixture was cooled to 0° C. Barium hydroxide octahydrate (3.14 g) was added thereto and the resulting mixture was stirred at 0° C. for 8 hours. The reaction solution was concentrated to remove THF, and water (150 ml) was added thereto, followed by washing the resulting mixture with ether. Aqueous layer was acidified by adding 1N hydrochloric acid in small portions thereto and extracted 3 times with ethyl acetate. Organic layers were washed with saturated brine and dried 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: chloroform/methanol=10/1). The obtained crude product was further purified by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=1/1→ethyl acetate) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid (6.15 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09162988B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-7d015e262b4541d1a628450748d8f32a
출처 메모uspto-grants-2015_10