Reacción #547925

ord-111032c9a5a246968d40918257e2d776

Ecuación de reacción

CC(=O)CCCCl
5-chloro-2-pentanone
CCO
ethanol
O=C([O-])[O-].[NH4+].[NH4+]
ammonium carbonate
[C-]#N.[K+]
potassium cyanide
CC1(CCCCl)NC(=O)NC1=O
5-(3-Chloropropyl)-5-methyl-2,4-imidazolidinedione

Disolventes

Condiciones de reacción

Temperatura
52.5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroequipped
  2. 2
    Temperaturawith reflux condenser and mechanical stirrer
  3. 3
    Temperaturacooled to 5-10° C.
  4. 4
    Otroexcess carbonate and cyanide was removed by the slow addition of 6 N aqueous hydrochloric acid (approx. 650 ml.) to pH 4
  5. 5
    workup.STIRRINGunder stirring
  6. 6
    ConcentraciónThe resulting mixture was concentrated to a volume of approximately 1 liter and refrigerated overnight
  7. 7
    FiltraciónThe crystalline deposit of 5-(3-chloropropyl)-5-methyl-2,4-imidazolidinedione was filtered off
  8. 8
    Otrodried

Procedimiento

To a stirred solution of 5-chloro-2-pentanone (87 g., 0.72 mol) in ethanol (750 ml.) contained in a 3-liter round-bottom flask, equipped with reflux condenser and mechanical stirrer was added a solution of ammonium carbonate (214 g.) in water (525 ml) followed by a solution of potassium cyanide (50 g.) in water (265 ml.). The mixture was stirred at 50-55° C. for 2.5 hours, cooled to 5-10° C. and excess carbonate and cyanide was removed by the slow addition of 6 N aqueous hydrochloric acid (approx. 650 ml.) to pH 4 under stirring. The resulting mixture was concentrated to a volume of approximately 1 liter and refrigerated overnight. The crystalline deposit of 5-(3-chloropropyl)-5-methyl-2,4-imidazolidinedione was filtered off, dried and recrystallized from chloroform/petroleum ether (25.1 g., 0.13 mol, 18%) m.p. 119-121° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04061542uspto-grants-1977_12