HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Cyano-2(R,S)-alpha-naphthoxybutyric acid | HCID 23049648 | — |
| Reactant | alpha-Naphthoxymalonic acid diethyl ester | HCID 54105534 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester | HCID 54279623 | — |
Reaction Steps
4-Cyano-2(R,S)-α-naphthoxybutyric acid: 0.11 ml of a 50% aqueous KOH solution is added at 0°, while stirring, to a mixture of 5.0 g of α-naphthoxymalonic acid diethyl ester and 1.09 ml of acrylonitrile. The reaction mixture is stirred for 5 days at room temperature and then dissolved in ethyl acetate. The ethyl acetate solution is washed with 2N sodium bicarbonate solution, 2N hydrochloric acid and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-cyanoethyl)-α-naphthoxymalonic acid diethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04727060 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-0c2d879632c7416297f9a04382172ffc |
| Source note | uspto-grants-1988_02 |