HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1-(8-Nonenyl)-3,7-dimethylxanthine | HCID 15230635 | — |
| Catalyst | tert-Butanol | HCID 6386 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(8,9-Dihydroxynonyl)-3,7-dimethylxanthine | HCID 9840808 | 54% |
Reaction Steps
A solution of 1-(8-nonenyl)-3,7-dimethylxanthine (810 mg, 2.7 mmol), 4-methylmorpholine-N- oxide (340 mg, 2.9 mmol) and 2.5% oxmium tetroxide in t-butanol (3 drops) in acetone (20 mL) and water (20 mL) was stirred for 24 hours. Saturated aqueous sodium dithionite solution (5 mL) was added. After stirring for 15 minutes, the reaction was extracted with 25% ethanol-dichloromethane (4×50 mL). The combined organic portions were dried over sodium sulfate, and the solvents were evaporated under vacuum. The solid residue was recrystallized (ethanol-chloroform), yielding 490 mg (54%) 1-(8,9-dihydroxynonyl)-3,7-dimethylxanthine (inventive compound no. 1561).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866576 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-62b5b1e8145b4eb698ed85aabb6b869f |
| Source note | uspto-grants-1999_02 |