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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495321Generated: October 25, 2026

Cyclohexanone → 2,6-Bis-(4-hexyloxy-benzylidene)-cyclohexanone

https://huagongshe.com/reaction/495321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium HydroxideHCID 14798—
Reactantp-(Hexyloxy)benzaldehydeHCID 79816—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2,6-Bis-(4-hexyloxy-benzylidene)-cyclohexanoneHCID 69497980—

Reaction Steps

Cyclohexanone (2.6 ml, 0.025 mol) was dissolved in ethanol (5 ml), and was added to sodium hydroxide (0.38 g, 0.01 mol) dissolved in water (6 ml) and ethanol (2 ml) and was left to stir for 20 min. 4-Hexyloxybenzaldehyde (10 ml, 0.048 mol), dissolved in ethanol (40 ml), was added and the mixture was stirred at room temperature for 16 h. A yellow crystalline solid was isolated by vacuum filtration and was washed with cold ethanol and dried in a vacuum oven. Yield=4.32 g, 36%. 1H NMR and 13C NMR showed expected signals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939479B2
Source datasetuspto-grants-2005_09
ORD IDord-affe587f4e1d4c599e66c79b12e2f716
Source noteuspto-grants-2005_09