HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 7-Benzyl-3,8-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,8-Dimethyl-3,7-dihydro-1H-purine-2,6-dione | HCID 17995918 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Benzyl-3,8-dimethylxanthine | HCID 14712608 | — |
Reaction Steps
A solution of sodium hydroxide (400 mg) in water (5 ml) was added to a suspension of 3,8-dimethylxanthine (1.80 g) in methanol (10 ml) at 70° C. and stirred for 1 hour. Benzyl bromide (1.2 ml) was added and the mixture was stirred at 70-80° C. for 5 hours. After evaporation of the solvent under reduced pressure, the residue was suspended in saturated aqueous ammonium chloride solution (50 ml) and extracted with ethyl acetate (3×75 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (30 ml), dried over magnesium sulfate and concentrate. The product was purified by recrystallization from ethanol. Yield=1.06 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075029 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-abed677c7c934476abfd167829b6f730 |
| Source note | uspto-grants-2000_06 |