化工社化工社 化学情報印刷レポート · 研究参考用
Norprostol → Methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Norprostol | HCID 3912664 | — |
| 反応物 | Gallium | HCID 5360835 | — |
| 反応物 | Boron | HCID 5462311 | — |
| 反応物 | Methyl 3-hydroxy-2-(3-methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl)-5-oxocyclopentaneheptanoate | HCID 21521708 | — |
| 反応物 | Tri(3methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl) aluminum | HCID 86733734 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | Methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03970683 |
| 出典データセット | uspto-grants-1976_07 |
| ORD ID | ord-fbc0dba1edb14fd3a2d083c0adf212e0 |
| 出典メモ | uspto-grants-1976_07 |