HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253352Generated: November 1, 2026
Methyl 4-oxocyclohexanecarboxylate → Methyl 4-oxocyclohexanecarboxylate
https://huagongshe.com/reaction/1253352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-oxocyclohexanecarboxylate | HCID 226643 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Product | Methyl 4-oxocyclohexanecarboxylate | HCID 226643 | — |
| Product | Methyl 4-(2-oxoethylidene)cyclohexane-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04748274 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-b757459c4ace472a86bd60e5e57e2fb9 |
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| Source note | uspto-grants-1988_05 |
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