HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(5-Hexenyl)-1-methyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methyluracil | HCID 12009 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-1-hexene | HCID 75906 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(5-Hexenyl)-1-methyluracil | HCID 23295874 | 72% |
Reaction Steps
3-(5,6-Oxidohexyl)-1-methyluracil was synthesized as follows: A mixture of sodium hydride (86 mg, 3.6 mmol) and 1-methyluracil (500 mg, 4 mmol) in dimethyl sulfoxide (25 ml) was stirred for 15 minutes, and then 6-bromo-1-hexene (647 mg, 4 mmol) was added. After stirring for 20 hours, the reaction mixture was poured into water (50 ml) and extracted with 20% ethanol-dichloromethane (3×50 ml). The combined organic layers were washed with saturated aqueous sodium chloride solution (20 ml) and dried over sodium sulfate. The solvent was evaporated under vacuum to give a residue which was purified by column chromatography (silica, ethyl acetate) to give 3-(5-hexenyl)-1-methyluracil (598 mg, 72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05824677 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-e77b89f329264e64ae7b569f33454724 |
| Source note | uspto-grants-1998_10 |