HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(7-Acetoxy-8-bromooctyl)-3,7-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(7,8-Dihydroxyoctyl)-3,7-dimethylxanthine | HCID 9797334 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(7-Acetoxy-8-bromooctyl)-3,7-dimethylxanthine | HCID 9823944 | 94% |
Reaction Steps
A mixture of 1-(7,8-dihydroxyoctyl)-3,7-dimethylxanthine, prepared as described above, (2.11 g, 6 mmol) was stirred with a 30% solution of hydrogen bromide in acetic acid (3.58 mL, 18 mmol) for 90 minutes. The mixture was then added to a flask containing aqueous sodium bicarbonate solution (4 g in 50 mL) and dichloromethane (30 mL). After 10 minutes of vigorous stirring the layers were separated and the aqueous portion was washed with dichloromethane (2×50 mL). The combined organic portions were dried over sodium sulfate and the solvent was evaporated under vacuum, yielding 2.51 g (94%) 1-(7-acetoxy-8-bromooctyl)-3,7-dimethylxanthine (inventive compound no. 1514) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866576 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-bb9555404b7a4502a29df100fc2d158c |
| Source note | uspto-grants-1999_02 |