HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Carbamoyl-2(R,S)-alpha-naphthoxybutyric acid | HCID 23049649 | — |
| Reactant | alpha-Naphthoxymalonic acid diethyl ester | HCID 54105534 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester | HCID 54384256 | — |
Reaction Steps
4-Carbamoyl-2(R,S)-α-naphthoxybutyric acid: 1.49 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene are added to a solution of 3 g of α-naphthoxymalonic acid diethyl ester (Example 36a) and 0.71 g of acrylamide in 5 ml of acetonitrile and the whole is stirred at room temperature for 24 hours. 25 ml of water are added to the reaction mixture, which is adjusted to pH 2 with 2N hydrochloric acid and extracted with ether. The ethereal phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-carbamoylethyl)-α-naphthoxymalonic acid diethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931591 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-fbeeed3d18824d14a975a3773f87247e |
| Source note | uspto-grants-1990_06 |