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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356452Generated: October 25, 2026

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

https://huagongshe.com/reaction/356452

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 numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-8e577549f35c46388dfd37bc0e3e764c
Source noteuspto-grants-1998_11