HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361486Generated: October 27, 2026
Carbon Dioxide → 1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthine
https://huagongshe.com/reaction/361486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(5,6-Dihydroxyhexyl)-3,7-dimethylxanthine | HCID 15895955 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Product | 1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthine | HCID 23295973 | 96% |
Reaction Steps
To 1-(5,6-dihydroxyhexyl)-3,7-dimethylxanthine 1.0 g, 3.38mmol) was added 30% hydrogen bromide-acetic acid (3.4 mL) over 30 seconds and then stirred for 2.5 hours until all of the solid dissolved. The solution was poured carefully over a mixture of sodium bicarbonate (12 g) and ice water (50 mL). After carbon dioxide evolution had subsided, the mixture was extracted with dichloromethane (3×25 mL). The combined extracts were dried over magnesium sulfate and the solvent evaporated under vacuum, yielding 1.3 g (3.24 mmol, 96%) 1-(5-Acetoxy-6-bromohexyl)-3,7-dimethylxanthine as a viscous oil, dissolved in methanol (5 mL). A 1M sodium methoxide in methanol solution (3.9 mL) was added over 30 seconds. After stirring for 20 minutes, the solution was reated with water (20 mL) and then extracted with dichloromethane (3×15 mL). The combined extracts were dried over magnesium sulfate and the solvents were evaporated under vacuum to yield 900 mg (3.24 mmol, 100% yield) 1-(5,6-Oxidohexyl)-3,7-dimethylxanthine as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05866576 |
|---|
| Source dataset | uspto-grants-1999_02 |
|---|
| ORD ID | ord-f822b9deae4846f3ad09e1ad4e4f3161 |
|---|
| Source note | uspto-grants-1999_02 |
|---|