Reacción #66040

ord-5aca40845e4e4632b7d57f0e39ef7216

Ecuación de reacción

CCCCCCCCCCCCCCCCCCCCCCOS(C)(=O)=O
1-docosanyl methanesulfonate
OCCOCCOCCOCCO
tetraethylene glycol
CC(C)(C)[O][K]
t-butoxypotassium
CCCCCCCCCCCCCCCCCCCCCCOCCOCCOCCOCCO
white crystal
CCCCCCCCCCCCCCCCCCCCCCOCCOCCOCCOCCO
tetraethylene glycol mono-1-docosanyl ether

Disolventes

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaafter cooling
  2. 2
    workup.STIRRINGthe mixture was stirred
  3. 3
    Filtración22.2 g of an insoluble matter was filtered
  4. 4
    ExtracciónAn ethyl acetate phase was extracted
  5. 5
    Otroseparated from the filtrate
  6. 6
    Concentraciónafter concentration under reduced pressure, 0.5 L of acetonitrile
  7. 7
    workup.ADDITIONwas added
  8. 8
    workup.STIRRINGthe mixture was stirred under ice cooling for one hour
  9. 9
    FiltraciónThe reaction mixture was filtered under reduced pressure
  10. 10
    Lavadowashed with 0.2 L of cold acetonitrile

Procedimiento

80.4 g of 1-docosanyl methanesulfonate was added to 207 mL of tetraethylene glycol, and the mixture was heated at 110° C. 40.0 g of t-butoxypotassium was gradually added over 2 hours. The mixture was further stirred for 3 hours, and after cooling, the reaction mixture was poured into 3 L of ice water, to which was then added 2 L of ethyl acetate, the mixture was stirred, and 22.2 g of an insoluble matter was filtered. An ethyl acetate phase was extracted and separated from the filtrate, after concentration under reduced pressure, 0.5 L of acetonitrile was added, and the mixture was stirred under ice cooling for one hour. The reaction mixture was filtered under reduced pressure and washed with 0.2 L of cold acetonitrile to obtain 81.6 g of a white crystal.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524644B2uspto-grants-2013_09