Reacción #430087

ord-40e3e127e5144d70bc12e02fa95da8b7

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas degassed
  2. 2
    Otroby bubbling nitrogen through the solution for 20 min
  3. 3
    workup.ADDITIONUnder nitrogen, tetrakistriphenylphosphinopalladium (0.468 g) was added
  4. 4
    TemperaturaAfter cooling
  5. 5
    workup.ADDITIONpyridine (5 ml) was added
  6. 6
    FiltraciónThe separated solids were filtered
  7. 7
    workup.ADDITIONthe filtrate diluted with an equal volume of water
  8. 8
    ExtracciónThe mixture was extracted with an equal volume of toluene
  9. 9
    Secadodried over magnesium sulfate
  10. 10
    Concentraciónconcentrated
  11. 11
    Otrochromatographed over 250 g of silica gel
  12. 12
    LavadoElution with 3:1 and 2:1 heptane

Procedimiento

A solution of 2-bromo-3,4-bis(decyloxy)-5-(benzothiazol-2-yl)-thiophene (12.2 g 20 mmol), and hexabutyl ditin (5.8 g, 10 mmol) in dioxane (100 ml), (freshly distilled from sodium after treatment with potassium hydroxide), was degassed by bubbling nitrogen through the solution for 20 min. Under nitrogen, tetrakistriphenylphosphinopalladium (0.468 g) was added and the mixture was heated at 100° C. for 20 hr. After cooling, pyridine (5 ml) was added and the resulting mixture allowed to stand for 1 hr. The separated solids were filtered and the filtrate diluted with an equal volume of water. The mixture was extracted with an equal volume of toluene, dried over magnesium sulfate and concentrated. The residue was combined with the initial solids and chromatographed over 250 g of silica gel. Elution with 3:1 and 2:1 heptane:toluene gave the desired product which was recrystallized from heptane to give 7.02 g (66.5% yield) mp 93.9°-95° C. Mass Spec. m/z 916 (M+ --C10H20). Elemental Analysis: Calculated for C62H92N2O4S4 : C, 70.36, H, 8.77, N, 2.65, and S, 12.10%. Found: C, 69.98, H, 8.90, N, 2.59, and S, 11.98 %.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05859251uspto-grants-1999_01