HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(5,6-Dihydroxyhexyl)-1-methylthymine
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-methylthymine | HCID 23295949 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-(5,6-Dihydroxyhexyl)-1-methylthymine | HCID 23287937 | 89% |
Reaction Steps
A solution of 3-(5-hexenyl)-1-methylthymine (2.00 g, 9 mmol), 4-methylmorpholine-N-oxide (1.17 mg, 10 mmol), and osmium tetroxide (0.15 ml of a 2.5% solution in t-butanol) in acetone (15 ml) and water (10 ml) was stirred for 20 hours. Saturated aqueous sodium hydrosulfite solution (10 ml) was added and after 15 minutes of stirring, 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 a solid residue. The solid was recrystallized (ethanol) to give 3-(5,6-dihydroxyhexyl)-1-methylthymine (2.00 g, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837703 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-fe0706512cca482cadf715233dd79734 |
| Source note | uspto-grants-1998_11 |