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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737171Generated: November 2, 2026

4-benzyl-2-cyclohexen-1-one → HCID 178521556, compound

https://huagongshe.com/reaction/1737171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-benzyl-2-cyclohexen-1-oneHCID 11769246—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 178521555HCID 178521555—
ProductHCID 178521556HCID 17852155690%

Reaction Steps

Besides, 30 g of the above-obtained 4-benzyl-2-cyclohexen-1-one were hydrogenated at room temperature for 6 hours using 5 g of Raney nickel in methanol under hydrogen pressure (3 kg/cm2) until the absorption of hydrogen was stopped. After an organic layer was collected by decantation and concentrated, the residue was purified by column chromatography, thereby obtaining 13 g of cis-4-benzylcyclo-hexanol and 14 g of trans-4-benzylcyclohexanol (yield: 90% in total).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962403
Source datasetuspto-grants-1999_10
ORD IDord-492ed2414c714ced9ae98803b82a15f4
Source noteuspto-grants-1999_10