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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67886Generated: October 25, 2026

Cyclohexanecarboxaldehyde → 1-Cyclohexyl-7-chloro-1-hepten-3-one

https://huagongshe.com/reaction/67886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
Reactant[(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chlorideHCID 73680070—
SolventO-XyleneHCID 7237—
Product1-Cyclohexyl-7-chloro-1-hepten-3-oneHCID 57214934—

Reaction Steps

2 parts of [(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chloride and 1.2 parts of cyclohexanecarbaldehyde were combined in 45 parts of xylene. This suspension was maintained under a nitrogen atmosphere and was refluxed for about 4 hours until a clear solution formed. After cooling the solution to room temperature, xylene was removed at a temperature of about 60° C. and under reduced pressure, leaving a product mixture. This mixture was separated chromatographically on a silica column using as the elution solvent 50 percent by volume of Skelly B in benzene, to yield 1-cyclohexyl-7-chloro-1-hepten-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04347192
Source datasetuspto-grants-1982_08
ORD IDord-192fe84647684fc38c7548455c798d5e
Source noteuspto-grants-1982_08