تفاعل #51146

ord-46bb61989247402b83f957372f1f9da2

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe temperature of the reaction mixture above 10° C
  2. 2
    درجة الحرارةthe temperature of the reaction was raised to 50-60° C.
  3. 3
    درجة الحرارةThe reaction was then cooled to 0° C.
  4. 4
    workup.ADDITIONAfter the addition
  5. 5
    workup.STIRRINGto stir at this temperature for 4 hours
  6. 6
    أخرىThe reaction mixture was transferred to a round bottom flask
  7. 7
    أخرىthe solvent was removed in vacuo
  8. 8
    أخرىWhen the solvent had been removed
  9. 9
    أخرىthe residue crystallized
  10. 10
    أخرىThe solid was triturated with heptane
  11. 11
    ترشيحfiltered

الإجراء التجريبي

A 5-Liter round bottom flask was charged with acetic anhydride (488 mL, 5.2 mol) and cooled to 0° C. Formic acid (240 mL, 6.4 mol) was then added at a rate that did not elevate the temperature of the reaction mixture above 10° C. After the formic acid was added, the temperature of the reaction was raised to 50-60° C. and stirred for 3 hours. The reaction was then cooled to 0° C. and 400 mL of THF was added. A solution of 4-bromoaniline (344 g, 2.0 mol) in 800 mL of THF was added dropwise. After the addition was complete, the reaction was allowed to stir at this temperature for 4 hours. The reaction was checked by thin-layer chromatography and found to be complete. The reaction mixture was transferred to a round bottom flask and the solvent was removed in vacuo. When the solvent had been removed, the residue crystallized. The solid was triturated with heptane and filtered. Obtained 396.8 grams of desired N-(4-bromo-phenyl)-formamide. Yield 99.2% The spectral properties of the solid were consistent with the desired material. Step (2): (4-bromo-phenyl)-methyl-amine

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849648B2uspto-grants-2005_02