HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-Allyloxybenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Allyloxybenzophenone | HCID 257910 | — |
Reaction Steps
4-Hydroxybenzophenone (100 parts) was dissolved in tetrahydrofuran (100 parts). Potassium hydroxide (30.9 parts) was added, heated and stirred until completely dissolved. Allyl chloride (46.4 parts) and potassium iodide (42 parts) were added to this solution. The mixture was refluxed for 8 hours. After cooling, it was washed with water and the solvent removed by distillation. A crude product of the desired 4-allyloxybenzophenone was obtained. It was recrystallized in n-hexane to obtain 110 parts of 4-allyloxybenzophenone (melting point 71° C.) at 72% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04467082 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-033a6afd5d024ad08e38130c84c05ddf |
| Source note | uspto-grants-1984_08 |