HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[2-(4-Toluenesulfonyloxy)propyl]pyridazine → 3-(2-Acetylthiopropyl)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[2-(4-Toluenesulfonyloxy)propyl]pyridazine | HCID 21265905 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(2-Acetylthiopropyl)pyridazine | HCID 15475352 | 69.5% |
Reaction Steps
3-[2-(4-Toluenesulfonyloxy)propyl]pyridazine (2.53 g) was dissolved in acetone (50 ml). To the solution was added potassium thioacetate (1.48 g), and the mixture was stirred for 4.5 hours under reflux. The reaction mixture was concentrated under reduced pressure. To the concentrate was added water (30 ml), which was subjected to extraction with ethyl acetate. The extract solution was dried over anhydrous magnesium sulfate, which was concentrated under reduced pressure. The concentrate was purified by a silica gel column chromatography (developing solvent: ethyl acetate-hexane 4:1→1:0) to afford the title compound (1.18 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174877B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-63e6186cf3db43dc8f18eda38f3904f1 |
| Source note | uspto-grants-2001_01 |