HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran → 4-(5-Oxo-3-hexadecynyl)-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran | HCID 15037106 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 4-(5-Oxo-3-hexadecynyl)-2-triethylsilylfuran | HCID 15037107 | — |
Reaction Steps
Jones reagent (a 2.6M solution in sulfuric acid, 0.13 ml, 0.36 mmol) was added dropwise to a solution of 4-(5-hydroxy-3-hexadecynyl)-2-triethylsilylfuran (136.4 mg, 0.33 mmol) in acetone (5 ml) at 0°. After 20 minutes, the excess Jones reagent was destroyed with ethanol (Ca 1 ml) and the mixture was diluted with water. The organic phase was separated, dried (magnesium sulfate) and evaporated down to give an oil, which was purified by preparative silica plates to give the titled ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059611 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-f486780a4f764b2fbb80c74641faa0a5 |
| Source note | uspto-grants-1991_10 |