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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547147생성일: 2026년 10월 26일

Sodium Hydroxide → (4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic Acid

https://huagongshe.com/reaction/547147

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Ammonium ChlorideHCID 25517—
반응물(4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic Acid Methyl EsterHCID 57709162—
용매MeOH tetrahydrofuranHCID 21899815—
생성물(4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic AcidHCID 5770911487.3%

반응 조건

온도60 °C

반응 단계

A 1 N sodium hydroxide aqueous solution (0.200 mL, 0.200 mmol) was added to a solution of (4′-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic acid methyl ester (Example 180-(2); 35.2 mg, 0.067 mmol) in methanol-tetrahydrofuran (1:1, 4 mL), and the mixture was stirred at 60° C. for two hours. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=10:1) to give the target compound as a colorless oil (30.1 mg, 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935688B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-b4e08a6db266429eb56691c6722f44d4
출처 메모uspto-grants-2011_05