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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861865Generated: October 30, 2026

Perchloric Acid → Benzenebutanoic acid, 4-cyclohexyl-

https://huagongshe.com/reaction/861865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerchloric AcidHCID 24247—
Reactant4-(4-Cyclohexylphenyl)-4-oxobutanoic acidHCID 161862—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
ProductBenzenebutanoic acid, 4-cyclohexyl-HCID 3041568102.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716944
Source datasetuspto-grants-1998_02
ORD IDord-8ad57db0acd24620ae9ed08cdc327bd0
Source noteuspto-grants-1998_02