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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253352Generated: November 1, 2026

Methyl 4-oxocyclohexanecarboxylate → Methyl 4-oxocyclohexanecarboxylate

https://huagongshe.com/reaction/1253352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-oxocyclohexanecarboxylateHCID 226643—
ReactantHCID 178418287HCID 178418287—
ProductMethyl 4-oxocyclohexanecarboxylateHCID 226643—
ProductMethyl 4-(2-oxoethylidene)cyclohexane-1-carboxylateHCID 14806116—

Reaction Steps

The epoxides used as the starting materials in the general process described above can be obtained from available starting materials using an appropriate series of reactions. Thus, methyl 4-hydroxybenzoate is hydrogenated using 5% rhodium on alumina as catalyst to give methyl 4-hydroxycyclohexanecarboxylate. This is then oxidized with pyridinium chlorochromate resulting in methyl 4-oxocyclohexanecarboxylate. The 2-carbon homologation of methyl 4-oxocyclohexanecarboxylate to give methyl 4-(oxoethylidene)cyclohexanecarboxylate is carried out using the method developed by A. I. Meyers. Acetaldehyde t-butylimine is metalated with lithium diisopropylamide and then treated with diethyl chlorophosphate to provide the lithioeneaminephosphonate. Addition of methyl 4-oxocyclohexanecarboxylate and subsequent acid hydrolysis gives methyl 4-(oxoethylidene)cyclohexanecarboxylate. The reduction of this oxoethylidene compound with sodium borohydride gives methyl 4-(2-hydroxyethylidene)cyclohexanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748274
Source datasetuspto-grants-1988_05
ORD IDord-b757459c4ace472a86bd60e5e57e2fb9
Source noteuspto-grants-1988_05