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HRID 517372作成日:2026年10月27日

Hydrochloric Acid → Fluprostenol

https://huagongshe.com/reaction/517372

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物Travoprost Impurity 26HCID 68031942—
溶媒IsopropanolHCID 3776—
生成物FluprostenolHCID 5311100—

反応条件

温度50 °C

反応手順

A solution of (8aR,9R,10R,11aS,Z)-10-hydroxy-9-((R,E)-3-hydroxy-4-(3-(trifluoromethyl)phenoxy) but-1-en-1-yl)-4,5,8,8a,9,10,11,11a-octahydrocyclopenta[b]oxecin-2(3H)-one (3.0 g from Example 8) in 2-propanol (25 mL) was treated with 3N potassium hydroxide aqueous solution (6.8 mL). This mixture was stirred at 50° C. for 2 hr. The reaction mixture was cooled and further adjusted with 3N hydrochloric acid aqueous solution to a pH of 8.5±0.2, and most of the solvent was removed under reduced pressure. The residue was diluted with saturated aqueous solution of sodium bicarbonate (20 mL) and ethyl acetate (20 mL). The mixture was stirred at room temperature for 5 minutes. The organic phase and the aqueous phase were separately collected. The aqueous layer was adjusted to a pH of 3.0±0.2 with 3N hydrochloric acid aqueous solution at room temperature and extracted with ethyl acetate (100 mL). The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to give 3.3 g of crude Travoprost acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115109B2
出典データセットuspto-grants-2015_08
ORD IDord-4d6952ea7a434117bbf3db8601ba1dd2
出典メモuspto-grants-2015_08