Reacción #54459

ord-2e7cef273a794ac795e7b088d974e437

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04148784uspto-grants-1979_04