Reacción #470376

ord-f4819e69156d4d829fe4a5907091e3f1

Ecuación de reacción

CC(C)N1CCCC1
N-isopropylpyrrolidine
CCOCCl
chloromethyl ethyl ether
CCOC[N+]1(C(C)C)CCCC1.[Cl-]
desired product
CCOC[N+]1(C(C)C)CCCC1.[Cl-]
N-Ethoxymethyl-N-Isopropylpyrrolidinium Chloride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was thereafter heated to a gradually elevated temperature
  2. 2
    Otrowhereby the reaction was terminated
  3. 3
    TemperaturaThe reaction mixture was cooled to 5° C.
  4. 4
    Filtraciónthe resulting solids were filtered off in nitrogen
  5. 5
    LavadoThe filter cake was washed with 200 ml of 2-butanone
  6. 6
    Lavadofurther washed with 200 ml of acetone
  7. 7
    Otrodried in a vacuum

Procedimiento

A 40.09 g quantity of N-isopropylpyrrolidine was dissolved in 361 g of dehydrated 2-butanone (reagent, product of Wako Pure Chemical Ind. Ltd.), followed by replacement with nitrogen. To the solution was added dropwise 33.54 g of chloromethyl ethyl ether (reagent, product of Tokyo Kasei Co., Ltd. as purified by distillation) at 5° C. over a period of 0.5 hour. The mixture was thereafter heated to a gradually elevated temperature and stirred at room temperature for 10 hours, whereby the reaction was terminated. The reaction mixture was cooled to 5° C., and the resulting solids were filtered off in nitrogen. The filter cake was washed with 200 ml of 2-butanone, further washed with 200 ml of acetone and dried in a vacuum, giving 55.72 g of the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08366956B2uspto-grants-2013_02