HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Iodohexane → HCID 15838316, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10171822 | HCID 10171822 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15838316 | HCID 15838316 | — |
Reaction Steps
To a solution of 17β-hydroxy-4-methyl-5α-4-azaandrostan-3-one (102 mg, 0.336 mmol) in DMSO (3 ml) was added powdered KOH (300 mg) followed by n-hexyliodide (400 μl). After stirring the reaction mixture overnight, the reaction was diluted with water and extracted with ethyl acetate. The organic layer was washed with water, then brine, then dried (MgSO4), and concentrated in vacuo. The residue was then purified by preparative thin layer chromatography to afford the title compound, characterized by H1NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693809 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-1751fb7c7ddd49c6abfb2d0db9b0ec09 |
| Source note | uspto-grants-1997_12 |