Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Xanthine → 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Xanthine | HCID 1188 | — |
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | 7-(6-Bromohexyl)-1,3-dimethylxanthine | HCID 20244073 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Acetic Anhydride | HCID 7918 | — |
| 생성물 | 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04576947 |
| 출처 데이터셋 | uspto-grants-1986_03 |
| ORD ID | ord-e571a2eb32c64f79b711437d06908a8a |
| 출처 메모 | uspto-grants-1986_03 |