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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003807Generated: October 25, 2026

Cyclohexyl methyl ketone → 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one

https://huagongshe.com/reaction/1003807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl methyl ketoneHCID 13207—
ReactantBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—
ReactantBarium hydroxideHCID 6093286—
SolventEthanolHCID 702—
Product3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-oneHCID 471477—

Reaction Steps

The title compound was prepared as described in General Method 2 using 17.40 g (138 mmol) of cyclohexyl methyl ketone, 29.26 g (138 mmol) of 4-benzyloxybenzaldehyde, 3.17 g of barium hydroxide (anhydrous), and 300 mL of 95% EtOH. The reaction was heated at reflux for eight hours. The crude product was recrystallized from EtOAc. The 25.85 g of product, contaminated with some 4-benzyloxybenzaldehyde, was taken on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046355
Source datasetuspto-grants-2000_04
ORD IDord-62c3f2b409b7437bb8b2f41c43f136a0
Source noteuspto-grants-2000_04