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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106965Generated: October 25, 2026

Hydrochloric Acid → (2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl ester

https://huagongshe.com/reaction/2106965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcrylamideHCID 6579—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Carbamoyl-2(R,S)-alpha-naphthoxybutyric acidHCID 23049649—
Reactantalpha-Naphthoxymalonic acid diethyl esterHCID 54105534—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931591
Source datasetuspto-grants-1990_06
ORD IDord-fbeeed3d18824d14a975a3773f87247e
Source noteuspto-grants-1990_06