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HRID 918273作成日:2026年10月25日

Norprostol → Methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate

https://huagongshe.com/reaction/918273

反応式

関与物質

役割名称HCID仕込み量
反応物NorprostolHCID 3912664—
反応物GalliumHCID 5360835—
反応物BoronHCID 5462311—
反応物Methyl 3-hydroxy-2-(3-methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl)-5-oxocyclopentaneheptanoateHCID 21521708—
反応物Tri(3methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl) aluminumHCID 86733734—
溶媒Acetic AcidHCID 176—
生成物Methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoateHCID 21521703—

反応手順

The 3-hydroxy-3-alkylated acetylenic compounds of this invention are prepared by employing the appropriately alkylated alkynyl boron, alkynyl gallium or alkynyl aluminum reactant. For example, treatment of methyl 3-hydroxy-5-oxocyclopent-1-eneheptanoate with tri(3methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl) aluminum, gallium or boron affords the epimeric methyl 3-hydroxy-2-(3-methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl)-5-oxocyclopentaneheptanoate. Typically, that compound may be hydrolyzed with a hydrolyzing agent such as hydrolytic acid, e.g. aqueous acetic acid, to yield the instant methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03970683
出典データセットuspto-grants-1976_07
ORD IDord-fbc0dba1edb14fd3a2d083c0adf212e0
出典メモuspto-grants-1976_07