HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(5,6-Dihydroxyhexyl)-1-methyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 3-(5-Hexenyl)-1-methyluracil | HCID 23295874 | — |
| Catalyst | tert-Butanol | HCID 6386 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(5,6-Dihydroxyhexyl)-1-methyluracil | HCID 23287950 | 66% |
Reaction Steps
A solution of 3-(5-hexenyl)-1-methyluracil (598 mg, 2.9 mmol), 4-methylmorpholine-N oxide (408 mg, 3,5 mmol), and a 2.5% solution of osmium tetroxide in t-butanol (3 drops) in acetone (15 ml) and water (5 ml) was stirred for 3 days. Saturated aqueous sodium hydrosulfite solution (10 ml) was added and the mixture was stirred for 15 minutes. Water (50 ml) was added and the mixture was extracted with 20% ethanol-dichloromethane (4×40 ml). The combined organic layers were dried over sodium sulfate and the solvents were evaporated under vacuum to give 3-(5,6-dihydroxyhexyl)-1-methyluracil (461 mg, 66% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05824677 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-d22c8b6d6b9a4117b69e0ca9496f8dd6 |
| Source note | uspto-grants-1998_10 |