HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 15230636 | HCID 15230636 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine | HCID 9819895 | 93% |
Reaction Steps
A solution of 1-(9-decenyl)-3,7-dimethylxanthine (3.2 g, 10.1 mmol), 4-methylmorpholine-N-oxide (1.41 g, 12 mmol) and a 2.5% solution in t-butanol of osmium tetroxide (3 drops) in acetone (40 mL) and water (10 mL) was stirred for 24 hours. Following addition of 5 mL of a saturated solution of sodium dithionite and an additional 15 minutes of stirring, the reaction product was extracted with 25% ethanol/dichloromethane (4×50 mL). The combined organic portions were dried over sodium sulfate. The solvents were evaporated to a give a white solid residue. Upon recrystallization of the residue in ethanol, 3.30 g (93% yield) 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine (inventive compound no. 1564) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866576 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-8aee9d66d06044828fbb51511a20c8bc |
| Source note | uspto-grants-1999_02 |