Reaktion #4689

ord-822d95ff4f2445239bc38f50ab6bd0a8

Reaktionsgleichung

NC(=O)CCC(Oc1cccc2ccccc12)C(=O)O
4-Carbamoyl-2(R,S)-α-naphthoxybutyric acid
C1CCC2=NCCCN2CC1
1,8-diazabicyclo[5.4.0]undec-7-ene
CCOC(=O)C(Oc1cccc2ccccc12)C(=O)OCC
α-naphthoxymalonic acid diethyl ester
C=CC(N)=O
acrylamide
Cl
hydrochloric acid
CCOC(=O)C(CCC(N)=O)(Oc1cccc2ccccc12)C(=O)OCC
(2-carbamoylethyl)-α-naphthoxymalonic acid diethyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ether
  2. 2
    WaschenThe ethereal phases are washed with water and brine
  3. 3
    Trocknendried over sodium sulphate
  4. 4
    Einengenconcentrated by evaporation

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04727060uspto-grants-1988_02