HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acrylate → Ethyl 3-(2-ethoxycarbonylethyl)amino-2,2-dimethylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Ethyl 3-amino-2,2-dimethylbutanoate | HCID 23283845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(2-ethoxycarbonylethyl)amino-2,2-dimethylbutanoate | HCID 23283843 | — |
Reaction Steps
In order to carry out this Michael addition, the ethyl 3-amino-2,2-dimethylbutanoate derivative 4 is dissolved with ethyl acrylate in a reaction medium which is inert under the reaction conditions chosen, preferably in a straight-chained or branched C1-4 -alkanol, most preferably ethanol, and heated, preferably to reflux temperature. After the reaction has taken place the solvent is eliminated in vacuo and the resulting ethyl 3-(2-ethoxycarbonylethyl)amino-2,2-dimethylbutanoate 5 is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140502 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-e36029eadf88402d84e9ce1159a782be |
| Source note | uspto-grants-2000_10 |