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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566158Generated: October 31, 2026

(4-Pentyl-1-cyclohexenyl)-3,5-difluorobenzene → (4-Pentyl-cyclohexyl)-3,5-difluorobenzene

https://huagongshe.com/reaction/566158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Pentyl-1-cyclohexenyl)-3,5-difluorobenzeneHCID 21265324—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
CatalystHCID 178418390HCID 178418390—
Product(4-Pentyl-cyclohexyl)-3,5-difluorobenzeneHCID 2224248891%

Reaction Steps

Mixture of (4-pentyl-1-cyclohexenyl)-3,5-difluorobenzene (89 mmol), Raney nickel (3.5 g), and 500 ml of Solmix was subjected to a hydrogenation reaction at room temperature under normal pressure for 10 hours. At the time when the amount of hydrogen has come not to further reduce and the reaction has come not to progress, catalyst was changed from Raney nickel to palladium carbon (2.4 g), and stirred for 8 hours. Palladium carbon was filtered off and the solvent was distilled off. The residue was purified by column chromatography (eluent: heptane) to give a (4-pentyl-cyclohexyl)-3,5-difluorobenzene (81 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174458B1
Source datasetuspto-grants-2001_01
ORD IDord-d79e2e89be8f4e63859aa237b0ae9ac1
Source noteuspto-grants-2001_01