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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761527Generated: October 25, 2026

Cyclodecanone → diethyl N-(1-cyclodecenyl)-aminomethylenemalonate

https://huagongshe.com/reaction/1761527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclodecanoneHCID 73918—
ReactantDiethyl (aminomethylidene)propanedioateHCID 226751—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventO-XyleneHCID 7237—
Productdiethyl N-(1-cyclodecenyl)-aminomethylenemalonateHCID 67906089—

Reaction Steps

A mixture of 25.0 g of cyclodecanone, 60.7 g of diethyl aminomethylenemalonate, 1.54 g of p-toluenesulfonic acid monohydrate in 500 ml xylene is refluxed 2 weeks under argon, collecting the distillate in a Dean-Stark trap. The solution is then decanted and solvent is removed. The residual oil is triturated twice with hexane and the combined hexane extract is concentrated to yield an oil which is flash chromatographed on 600 g of silica gel using 99:1 methylene chloride ethyl acetate as eluent. A forerun containing cyclodecanone is discarded and the fractions containing the product are combined and concentrated to dryness to give diethyl N-(1-cyclodecenyl)-aminomethylenemalonate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826854
Source datasetuspto-grants-1989_05
ORD IDord-192731807edd42b9ba01020ec4633ce5
Source noteuspto-grants-1989_05