戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1706376作成日:2026年10月27日

Sodium hydride → 1,3-Dimethyl-7-(5-methyl-hex-5-enyl)-xanthine

https://huagongshe.com/reaction/1706376

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物LomifyllineHCID 65599—
反応物MethylenetriphenylphosphoraneHCID 137960—
反応物Methyltriphenylphosphonium iodideHCID 638159—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1,3-Dimethyl-7-(5-methyl-hex-5-enyl)-xanthineHCID 12807384—

反応条件

温度80 °C

反応手順

0.5 g of sodium hydride are reacted with 15 ml of anhydrous dimethyl-sulphoxide under a nitrogen atmosphere with stirring at 80° C. and cooled to 15° C. after 25 minutes. To prepare triphenyl-methylene-phosphorane, 8.1 g of methyl-triphenyl phosphonium iodide in 20 ml of anhydrous dimethyl-sulphoxide are added to this solution. After stirring for 10 minutes at room temperature, 5.6 g of 1,3-dimethyl-7-(5-oxohexyl)-xanthine in 10 ml of dimethylsulphoxide are added dropwise over 10 minutes, and the temperature is not allowed to exceed 20° C. After standing overnight, the mixture is dissolved in water, extracted with diethyl ether and the ether phase is separated and dried over Na2SO4. The product obtained after evaporation at reduced pressure is subsequently subjected to a purification by column chromatography on silica gel with methylene chloride/acetone (1:1) as eluent. The resulting product is in the form of an oil after distillation under reduced pressure. Yield: 3.5 g (63.3% of theory relative to the starting product used); refractive index: nD20 =1.5445.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04207321
出典データセットuspto-grants-1980_06
ORD IDord-e12a492265e849b391491de412a086cb
出典メモuspto-grants-1980_06