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Xanthine → 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Xanthine | HCID 1188 | — |
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | 7-(6-Bromohexyl)-1,3-dimethylxanthine | HCID 20244073 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Acetic Anhydride | HCID 7918 | — |
| 生成物 | 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04576947 |
| 出典データセット | uspto-grants-1986_03 |
| ORD ID | ord-e571a2eb32c64f79b711437d06908a8a |
| 出典メモ | uspto-grants-1986_03 |