HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 7-(6-Bromohexyl)-1,3-dimethylxanthine | HCID 20244073 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,3-Dimethyl-7-(6-hydroxyhexyl)-xanthine | HCID 10802704 | 90% |
Reaction Steps
3.4 g of 1,3-dimethyl-7-(6-bromohexyl)-xanthine are boiled overnight under reflux in 50 ml of glacial acetic acid to which 1 ml of acetic anhydride and 5 g of potassium acetate have been added. After evaporated of the solvent by distillation in vacuo the residue is dissolved in 50 ml of 5% sulfuric acid on the addition of 20 ml methanol. The solution is boiled under reflux for 1 hour. The mixture is extracted with chloroform. The chloroform phase is washed until it is neutral and concentrated in vacuo. 1,3-dimethyl-7-(6-hydroxyhexyl)-xanthine having a melting point of 80° C. is obtained in a yield of more than 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576947 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-74c7a12f4bbb44fa86d84aa4afa36074 |
| Source note | uspto-grants-1986_03 |