HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-(4-Acetyl-3-hydroxy-2-propylphenylthio)butylbromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Hydroxy-3-propyl-4-sulfanylphenyl)ethan-1-one | HCID 13295518 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(4-Acetyl-3-hydroxy-2-propylphenylthio)butylbromide | HCID 15712384 | 52.6% |
Reaction Steps
To a refluxing mixture of 1.4-dibromobutane (32.9 g), anhydrous potassium carbonate (5.25 g) and potassium iodide (1 g) in acetone (100 ml) was added dropwise a solution of 2'-hydroxy-4'-mercapto-3'-propylacetophenone (8.00 g) in acetone (20 ml) during an hour and refluxed for 2 hours. The mixture was filtered off and the solvent was evaporated. The resulting residue was purified by silica gel column chromatography, eluting with benzene, to give the title compound (6.90 g, 52.6 %) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04942245 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-6b8f82f9dd2b41a1bf65120175688d3d |
| Source note | uspto-grants-1990_07 |