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HRID 258813作成日:2026年10月25日

Ethyl Bromide → Vinpocetine

https://huagongshe.com/reaction/258813

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物Potassium HydroxideHCID 14797—
反応物(+)-Apovincaminic acidHCID 160154—
溶媒EthanolHCID 702—
生成物VinpocetineHCID 44395566%

反応手順

1 g. (0.0031 moles) of apovincaminic acid and 0.17 g. (0.003 moles) of potassium hydroxide are dissolved in 80 ml. of anhydrous ethanol, thereafter 0.4 g. (0.0036 moles) of ethyl bromide are added to the solution. The solution is boiled under reflux for 3 hours. The reaction is monitored by layer chromatography. The solution is cooled and evaporated to dryness under reduced pressure. The dry residue is dissolved in 500 ml. of 2% aqueous sulfuric acid, and the solution is filtered. The pH of the filtrate is adjusted to 8 with 5% aqueous sodium hyrodxide solution. A small amount of precipitate separates. The mixture is extracted with 200 ml. portions of methylene chloride until no positive Mayer reaction can be observed in the aqueous phase. The organic phases are separated, combined, dried over anhydrous potassium carbonate, filtered and evaporated to dryness under reduced pressure. The dry residue is dissolved in 10 ml. of anhydrous ethanol, and the solution is left to crystallize at 0° to 2° C for 10 hours. 0.66 g. of apovincaminic acid ethyl ester are obtained (yield: 66%). On the basis of layer chromatography, a uniform product is formed. M.p.: 144° C (Boetius).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04035370
出典データセットuspto-grants-1977_07
ORD IDord-311fcc7f5b0a4a26b9fb8000e103174e
出典メモuspto-grants-1977_07