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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4593Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/4593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAcrylamideHCID 6579—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt4-Carbamoyl-2(R,S)-alpha-naphthoxybutyric acidHCID 23049649—
Eduktalpha-Naphthoxymalonic acid diethyl esterHCID 54105534—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt(2-Carbamoylethyl)-alpha-naphthoxymalonic acid diethyl esterHCID 54384256—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04727060
Quelldatensatzuspto-grants-1988_02
ORD IDord-822d95ff4f2445239bc38f50ab6bd0a8
Quellennotizuspto-grants-1988_02