HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Ibuprofen, (+-)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1-[4-(2-Methylpropyl)phenyl]ethan-1-ol | HCID 181654 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Rhodium(III) iodide | HCID 4428348 | — |
| Catalyst | Hastelloy C | HCID 11332432 | — |
| Product | Ibuprofen, (+-)- | HCID 3672 | — |
Reaction Steps
A 300-ml autoclave made of Hastelloy C was charged with 1.5 g (3.10 mmol) of rhodium iodide and 100 ml of dioxane, as a solvent, to cause a reaction to occur therein under a hydrogen pressure of 10 kg/cm2 and a carbon monoxide pressure of 30 kg/cm2 at 150° C. with stirring. After cooling the reaction mixture and relieving the pressure, 8.9 g (50.0 mmol) of α-(4-isobutylphenyl)ethyl alcohol and 0.40 g (3.15 mmol) of iodine were further added thereto and then the procedure of Example 1 was repeated. Thus 4.5 g of α-(4-isobutylphenyl)propionic acid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04843172 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-ba8d917c913a443fa1d50ef643c4aa16 |
| Source note | uspto-grants-1989_06 |