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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245603생성일: 2026년 10월 26일

Potassium Hydroxide → Treprostinil

https://huagongshe.com/reaction/245603

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물2-((1R,2R,3aS,9aS)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-((S,E)-3-hydroxyoct-1-enyl)-1H-cyclopenta[b]naphthalen-5-yloxy)acetic acidHCID 71268573—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물TreprostinilHCID 691814088%

반응 단계

2-((1R,2R,3aS,9aS)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-((S,E)-3-hydroxyoct-1-enyl)-1H-cyclopenta[b]naphthalen-5-yloxy)acetic acid (2.5 g, 0.008 mol) in dry methanol (25 ml) was treated with potassium hydroxide (0.5 g, 0.008 mol), then with 5% Pd/C (0.5 g, 20% wt) under hydrogen overnight at room temperature. Then, the reaction mixture was filtered with celite pad. The solvent was evaporated off under vacuum. The residues was diluted with 50 nm ethyl, acetate and 50 ml saturated sodium bicarbonate aqueous. The mixture was phase separated and the organic layers was extracted with 50 ml saturated sodium bicarbonate aqueous. The aqueous layers were combined and then 3N HCl was added slowly until pH=˜2. The aqueous layer was extracted with 100 ml ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The solid was filtered off. The solvent was evaporated off under vacuum. The crude product was purified by crystallization. The titled compound was obtained in a crystalline form. Yield: 88%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658837B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-07838bb9c2c34183a21f60bf44159cb6
출처 메모uspto-grants-2014_02