Reaktion #54459

ord-2e7cef273a794ac795e7b088d974e437

Reaktionsgleichung

O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC1(C)CC(=O)CC(C)(C)N1
triacetonamine
CCOC(=O)CC#N
ethyl cyanoacetate
CC(=O)[O-].[NH4+]
ammonium acetate
CCOC(=O)C(C#N)=C1CC(C)(C)NC(C)(C)C1
Ethyl 2,2,6,6-tetramethyl-4-piperidinylidene-cyanoacetate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux for 1.5 hours under a water separator
  2. 2
    Trocknenthe organic phase is dried over sodium sulphate

Vorschrift

155 g (1 mol) of triacetonamine, 113 g of ethyl cyanoacetate, 300 ml of benzene and 31 g of ammonium acetate are kept under reflux for 1.5 hours under a water separator. The benzene phase is treated with 50% of potassium carbonate, the organic phase is dried over sodium sulphate and the benzene is then stripped off in vacuo. Ethyl 2,2,6,6-tetramethyl-4-piperidinylidene-cyanoacetate is obtained as an oily residue.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04148784uspto-grants-1979_04