Reacción #66039

ord-200439b3128a40c29f876c8dc27b0512

Ecuación de reacción

CS(=O)(=O)Cl
methanesulfonyl chloride
CCCCCCCCCCCCCCCCCCCCCCO
behenyl alcohol
CCN(CC)CC
triethylamine
CCCCCCCCCCCCCCCCCCCCCCOS(C)(=O)=O
white crystal
CCCCCCCCCCCCCCCCCCCCCCOS(C)(=O)=O
1-docosanyl methanesulfonate

Disolventes

Condiciones de reacción

Temperatura
40°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGfurther stirred for 30 minutes
  2. 2
    workup.ADDITIONthe resulting mixture was ultrasonically dispersed for 15 minutes
  3. 3
    workup.STIRRINGfurther stirred at room temperature for 4 hours
  4. 4
    FiltraciónThe dispersion was filtered under reduced pressure
  5. 5
    Lavadoa crystal was washed with 2 L of water
  6. 6
    workup.STIRRINGThe resulting white crystal was stirred in 1.5 L of acetonitrile for one hour
  7. 7
    Filtraciónfiltered under reduced pressure
  8. 8
    Lavadowashed with 0.5 L of acetonitrile
  9. 9
    OtroThe resulting crystal was dried under reduced pressure

Procedimiento

247.4 g of behenyl alcohol (1-docosanol) was dissolved in 640 mL of tetrahydrofuran, 116.1 mL of methanesulfonyl chloride was gradually added, and 64.7 mL of triethylamine was then added dropwise under ice cooling over 30 minutes. After stirring for one hour, the mixture was heated at 40° C. and further stirred for 30 minutes. The reaction mixture was poured into 3.5 L of ice water, and the resulting mixture was ultrasonically dispersed for 15 minutes and further stirred at room temperature for 4 hours. The dispersion was filtered under reduced pressure, and a crystal was washed with 2 L of water. The resulting white crystal was stirred in 1.5 L of acetonitrile for one hour, filtered under reduced pressure and then washed with 0.5 L of acetonitrile. The resulting crystal was dried under reduced pressure to obtain 303.4 g of a white crystal.

Fuente

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