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HRID 482882作成日:2026年10月26日

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

https://huagongshe.com/reaction/482882

反応式

関与物質

役割名称HCID仕込み量
反応物XanthineHCID 1188—
反応物Potassium IodideHCID 4875—
反応物Potassium AcetateHCID 517044—
反応物7-(6-Bromohexyl)-1,3-dimethylxanthineHCID 20244073—
溶媒Acetic AcidHCID 176—
溶媒Acetic AnhydrideHCID 7918—
生成物1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthineHCID 10802704—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04576947
出典データセットuspto-grants-1986_03
ORD IDord-e571a2eb32c64f79b711437d06908a8a
出典メモuspto-grants-1986_03