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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720743Generated: November 1, 2026

Cyclohexyl methyl ketone → HCID 54220593, compound

https://huagongshe.com/reaction/1720743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl methyl ketoneHCID 13207—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 54220593HCID 5422059369.6%

Reaction Steps

A sodium ethoxide solution (21% by weight in ethanol, 6.805 gm, 21 mmol) was added to a mixture of 1-cyclohexyl-1-ethanone (18.749 g, 140 mmol, from Aldrich) and 4-fluorobenzaldehyde (17.37 g, 140 mmol, from Aldrich) in ethanol (100 ml), stirring under argon. The solution was allowed to stir 1.5 hours. The reaction mixture was then concentrated to afford an orange oil. The oil was dissolved in ether, washed with saturated NH4Cl and brine, then dried over Na2SO4, filtered and concentrated to an orange oil. The oil was purified by distillation (bp=143° C. at 1.3 mm Hg). The resultant yellowish oil slowly solidified to afford the title compound as hard yellow crystals (22.640 gm, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506219
Source datasetuspto-grants-1996_04
ORD IDord-d509d0468a1243b698357f3d2003fdd4
Source noteuspto-grants-1996_04