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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482882생성일: 2026년 10월 25일

Xanthine → 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine

https://huagongshe.com/reaction/482882

반응식

참여 물질

역할이름HCID투입량
반응물XanthineHCID 1188—
반응물Potassium IodideHCID 4875—
반응물Potassium AcetateHCID 517044—
반응물7-(6-Bromohexyl)-1,3-dimethylxanthineHCID 20244073—
용매Acetic AcidHCID 176—
용매Acetic AnhydrideHCID 7918—
생성물1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthineHCID 10802704—

반응 단계

1,3-dimethyl-7-(6-bromohexyl)-xanthine is refluxed overnight with a sixfold molar excess of potassium acetate with the addition of catalytic quantities, such as 2 mol percent, referred to the xanthine, of potassium iodide in a mixture of 5 ml of acetic anhydride and 200 ml of glacial acetic acid. The solvent is evaporated in vacuo. The residue is dissolved in water and the pH of the solution is adjusted to a value of 7 with 4N sodium hydroxide. The solution is then extracted with chloroform. The isolated 1,3-dimethyl-7-(acetoxyhexyl)-xanthine is subsequently hydrolysed to the corresponding hydroxyalkyl compound by boiling with 5% sulfuric acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04576947
출처 데이터셋uspto-grants-1986_03
ORD IDord-e571a2eb32c64f79b711437d06908a8a
출처 메모uspto-grants-1986_03