HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perchloric Acid → Benzenebutanoic acid, 4-cyclohexyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 4-(4-Cyclohexylphenyl)-4-oxobutanoic acid | HCID 161862 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzenebutanoic acid, 4-cyclohexyl- | HCID 3041568 | 102.7% |
Reaction Steps
A solution of 3-(4-cyclohexylbenzoyl)propionic acid (10.7 g), acetic acid (100 ml) and perchloric acid (2.3 ml) was hydrogenated in the presence of 5% palladium carbon (50% wet, 3.0g) at room temperature under ordinary pressure. After removal of the catalyst by filtration, the filtrate was concentrated under reduced pressure. After water (100 ml) was added, the residue was extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine, and dried (MgSO4), after which the solvent was evaporated off, to yield 4-(4-cyclohexylphenyl)butyric acid (10.4 g, 100%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716944 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-8ad57db0acd24620ae9ed08cdc327bd0 |
| Source note | uspto-grants-1998_02 |