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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1706376생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1706376

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물LomifyllineHCID 65599—
반응물MethylenetriphenylphosphoraneHCID 137960—
반응물Methyltriphenylphosphonium iodideHCID 638159—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1,3-Dimethyl-7-(5-methyl-hex-5-enyl)-xanthineHCID 12807384—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04207321
출처 데이터셋uspto-grants-1980_06
ORD IDord-e12a492265e849b391491de412a086cb
출처 메모uspto-grants-1980_06