Reacción #1885007

ord-5df328fe7cfa4ae9b7e0828bec02fd12

Ecuación de reacción

[Cl][Sn]([Cl])([Cl])[Cl]
tin chloride
CCCCc1ccc(N)cc1
4-n-butylaniline
O=N[O-].[Na+]
Sodium nitrite
CCCCc1ccc(NN)cc1
solid
Rendimiento 66.0%
CCCCc1ccc(NN)cc1
p-Butylphenylhydrazine
Rendimiento 66.0%

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled
  2. 2
    workup.ADDITIONwas added slowly
  3. 3
    workup.STIRRINGthe resulting suspension was stirred at 0° C. for 3 h
  4. 4
    FiltraciónThe solid was filtered
  5. 5
    workup.DISSOLUTIONdissolved in a mixture of 40% potassium hydroxide solution (200 mL) and ethyl acetate (200 mL)
  6. 6
    OtroThe organic layer was separated
  7. 7
    Extracciónthe aqueous layer was further extracted with ethyl acetate
  8. 8
    LavadoThe combined organic extracts were washed with 10% hydrochloric acid (120 mL)
  9. 9
    Filtraciónthe solid was filtered
  10. 10
    OtroThe organic layer was separated
  11. 11
    Secadodried over Na2SO4
  12. 12
    Otrothe solvent was evaporated
  13. 13
    OtroThe resulting solid was recrystallized from ethanol

Procedimiento

Sodium nitrite (11.74 g, 0.17 mol) in water (50 mL) was added over 30 min to an ice-cooled and stirred suspension of 4-n-butylaniline (24.30 g, 0.16 mol) in 6 N hydrochloric acid (190 mL). After an additional 15 min, a suspension of tin chloride dehydrate (108.3 g, 0.4 mol) in 6 N hydrochloric acid (190 mL) was added slowly, and the resulting suspension was stirred at 0° C. for 3 h. The solid was filtered and dissolved in a mixture of 40% potassium hydroxide solution (200 mL) and ethyl acetate (200 mL). The organic layer was separated and the aqueous layer was further extracted with ethyl acetate. The combined organic extracts were washed with 10% hydrochloric acid (120 mL), a solid started to develop in the organic layer. After cooled it to 0° C., the solid was filtered. The organic layer was separated, dried over Na2SO4, and the solvent was evaporated. The resulting solid was recrystallized from ethanol to afford a white solid (17.35 g, 54%). 1H NMR (300 MHz, DMSO-d6): δ 10.18 (s, 3H), 7.10 (d, 2H, J=8.4 Hz), 6.92 (d, 2H, J=8.7 Hz), 2.51 (t, 2H, J=7.5 Hz), 1.50 (pentet, 2H, J=7.5 Hz), 1.27 (sextet, 2H, J=7.8 Hz), 0.88 (t, 3H, J=7.5 Hz).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08343636B2uspto-grants-2013_01