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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253353Generated: November 1, 2026

Diethyl chlorophosphate → Methyl 4-(2-oxoethylidene)cyclohexane-1-carboxylate

https://huagongshe.com/reaction/1253353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantN-Ethylidene-2-methylpropan-2-amineHCID 138901—
ReactantMethyl 4-oxocyclohexanecarboxylateHCID 226643—
ReactantLithium diisopropylamideHCID 2724682—
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-03f4d275c25b414882dc8d9bdd405c13
Source noteuspto-grants-1988_05