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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737175Generated: November 1, 2026

2-Benzylidenecyclohexanone → HCID 12118799, compound

https://huagongshe.com/reaction/1737175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BenzylidenecyclohexanoneHCID 98926—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 12118799HCID 1211879988%
ProductCyclohexanol, 2-(phenylmethyl)-, cis-HCID 12283992—

Reaction Steps

Then, 10 g of 2-benzylidenecyclohexanone were hydrogenated at room temperature using 1 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 4.6 g of cis-2-benzylcyclohexanol and 4.4 g of trans-2-benzylcyclohexanol (yield: 88% in total).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962403
Source datasetuspto-grants-1999_10
ORD IDord-66b69874a6dd4b8db91e126567b090d3
Source noteuspto-grants-1999_10