HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclodecanone → diethyl N-(1-cyclodecenyl)-aminomethylenemalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclodecanone | HCID 73918 | — |
| Reactant | Diethyl (aminomethylidene)propanedioate | HCID 226751 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | diethyl N-(1-cyclodecenyl)-aminomethylenemalonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04826854 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-192731807edd42b9ba01020ec4633ce5 |
| Source note | uspto-grants-1989_05 |