Reacción #1810789

ord-4a566be5af11461bb439be881d3227b2

Ecuación de reacción

CCCCCCOc1cscc1OCCCCCC
3,4-dihexoxythiophene
c1ccsc1
thiophene
O=S(=O)(O)O
sulfuric acid
O=C(O)COCC(O)=S
thiodiglycolic acid
CCOC(=O)COCC(=S)OCC
thiodiglycolic acid diethylester
Rendimiento 90.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto prepare a reaction solution
  2. 2
    Temperaturathe reaction solution was refluxing
  3. 3
    Temperaturaunder heating for 12 hr
  4. 4
    OtroSubsequently, substantially 500 mL of water and ethanol was removed from the reaction solution
  5. 5
    workup.ADDITIONFurthermore, 400 mL of ethanol was added
  6. 6
    Temperaturaafter refluxing
  7. 7
    Temperaturaunder heating for 20 hr
  8. 8
    workup.ADDITIONthe reaction solution was added water
  9. 9
    Extracciónto extract with ether
  10. 10
    SecadoA layer of ether was dried with magnesium sulfate
  11. 11
    Filtraciónby filtering
  12. 12
    Concentraciónconcentrating
  13. 13
    workup.DISTILLATIONThe residue was distilled under reduced pressure of 200 Pa

Procedimiento

An example of synthesizing 3,4-dihexoxythiophene as a thiophene monomer is shown below. 2 mL of sulfuric acid was added in an ethanol solution (800 mL) of thiodiglycolic acid (250 g, 1.67 mol) to prepare a reaction solution, then the reaction solution was refluxing under heating for 12 hr after stirring for 24 hr. Subsequently, substantially 500 mL of water and ethanol was removed from the reaction solution according to azeotropy. Furthermore, 400 mL of ethanol was added and after refluxing under heating for 20 hr, the reaction solution was added water to extract with ether. A layer of ether was dried with magnesium sulfate, followed by filtering and concentrating. The residue was distilled under reduced pressure of 200 Pa and a temperature of 100 to 110 degree centigrade, and thereby thiodiglycolic acid diethylester was obtained at a yield of 90 percent.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07485375B2uspto-grants-2009_02