تفاعل #487560

ord-58002ebafbbe4bd491326213a4052320

معادلة التفاعل

[I-].[K+]
potassium iodide
O=S(=O)(O)O
sulfuric acid
CCc1ccc(Br)cc1N
5-bromo-2-ethylaniline
O=N[O-].[Na+]
sodium nitrite
CCc1ccc(Br)cc1I
4-bromo-1-ethyl-2-iodobenzene

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةby brief heating
  2. 2
    درجة الحرارةat reflux until dissolution
  3. 3
    أخرىproducing a fine precipitate
  4. 4
    درجة الحرارةfurther cooled to approximately 0° C. in an ice/salt bath
  5. 5
    درجة الحرارةmaintaining a temperature below 5° C.
  6. 6
    ترشيحThe reaction mixture is next filtered
  7. 7
    workup.ADDITIONAfter the addition
  8. 8
    درجة الحرارةis briefly heated to 80° C.
  9. 9
    درجة الحرارةto cool to room temperature again
  10. 10
    استخلاصThe reaction mixture is extracted with ethyl acetate (3×50 ml)
  11. 11
    غسيلthe organic phase is washed with 1M aqueous hydrochloric acid (30 ml) and aqueous sodium thiosulfate (2×30 ml)
  12. 12
    تجفيفAfter drying over anhydrous magnesium sulfate and concentration in vacuo 4-bromo-1-ethyl-2-iodobenzene (4.90 g)
  13. 13
    أخرىis furnished as an orange liquid

الإجراء التجريبي

To a stirred mixture of 5-bromo-2-ethylaniline (3.39 g, 200 mmol) in distilled water (110 ml) is added concentrated sulfuric acid (5.60 ml), followed by brief heating at reflux until dissolution. The mixture is allowed to cool to room temperature, producing a fine precipitate, then further cooled to approximately 0° C. in an ice/salt bath. To this slurry is added an aqueous solution of sodium nitrite (1.17 g, 16.94 mmol) in distilled water (10 ml) dropwise over 15 minutes, maintaining a temperature below 5° C., followed by additional stirring for 30 minutes. The reaction mixture is next filtered then added to a second solution of aqueous potassium iodide (8.44 g, 50.83 mmol) in distilled water (45 ml) dropwise at room temperature. After the addition is complete the solution is briefly heated to 80° C. then allowed to cool to room temperature again. The reaction mixture is extracted with ethyl acetate (3×50 ml), and the organic phase is washed with 1M aqueous hydrochloric acid (30 ml) and aqueous sodium thiosulfate (2×30 ml). After drying over anhydrous magnesium sulfate and concentration in vacuo 4-bromo-1-ethyl-2-iodobenzene (4.90 g) is furnished as an orange liquid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741806B2uspto-grants-2014_06