Rosenmund–von Braun reaction

The Rosenmund–von Braun synthesis is an organic reaction in which an aryl halide reacts with cuprous cyanide to an aryl nitrile.[1][2][3]

The reaction was named after Karl Wilhelm Rosenmund who together with his Ph.D. student Erich Struck discovered in 1914 that aryl halide reacts with alcohol water solution of potassium cyanide and catalytic amounts of cuprous cyanide at 200°C. The reaction yields the carboxylic acid, not the nitrile, but Rosenmund speculated that the intermediate should be the nitrile.[1] Independently Alfred Pongratz[4] and Julius von Braun[2] improved the reaction by changing the reaction conditions to higher temperatures and used no solvent for the reaction. Further improvement of the reaction was done in the following years,[5] for example the use of ionic liquids as solvent for the reaction.[6]

Other example

See Also

References

  1. ↑ 1.0 1.1 Rosenmund, Karl W.; Struck, Erich (27 September 1919). "Das am Ringkohlenstoff gebundene Halogen und sein Ersatz durch andere Substituenten. I. Mitteilung: Ersatz des Halogens durch die Carboxylgruppe". Berichte der deutschen chemischen Gesellschaft (A and B Series) 52 (8): 1749–1756. doi:10.1002/cber.19190520840.
  2. ↑ 2.0 2.1 v. Braun, Julius; Manz, Gottfried (1931). "Fluoranthen und seine Derivate. III. Mitteilung". Justus Liebig's Annalen der Chemie 488 (1): 111–126. doi:10.1002/jlac.19314880107.
  3. ↑ E. Callen, Joseph; A. Dornfeld, Clinton; H. Coleman, George (1948). "9-CYANOPHENANTHRENE". Organic Syntheses (28): 34. doi:10.15227/orgsyn.028.0034.
  4. ↑ Pongratz, Alfred (July 1927). "Untersuchungen �ber Perylen und seine Derivate". Monatshefte f�r Chemie 48 (7): 585–591. doi:10.1007/BF01518076.
  5. ↑ KOELSCH, C. F.; WHITNEY, A. G. (November 1941). "THE ROSENMUND-von BRAUN NITRILE SYNTHESIS". The Journal of Organic Chemistry 06 (6): 795–803. doi:10.1021/jo01206a002.
  6. ↑ Wu, Jeff Xin; Beck, Brandon; Ren, Rex X. (January 2002). "Catalytic Rosenmund–von Braun reaction in halide-based ionic liquids". Tetrahedron Letters 43 (3): 387–389. doi:10.1016/S0040-4039(01)02168-2.