Wilhelm Rudolph Fittig

Wilhelm Rudolph Fittig (6 December 1835 – 19 November 1910) was a German chemist. Fittig discovered the pinacol coupling reaction, mesitylene, diacetyl and biphenyl. He studied the action of sodium on ketones and hydrocarbons. He discovered the Fittig reaction or Wurtz–Fittig reaction for the synthesis of alkylbenzenes, he proposed a diketone structure for benzoquinone and isolated phenanthrene from coal tar. He discovered and synthesized the first lactones and investigated structures of piperine naphthalene and fluorene.[1]

Wilhelm Rudolph Fittig
Wilhelm Rudolph Fittig
Born(1835-12-06)6 December 1835
Hamburg, Germany
Died19 November 1910(1910-11-19) (aged 74)
Strasbourg, France
NationalityGerman
Alma materUniversity of Göttingen
Known forFittig reaction
AwardsDavy Medal (1906)
Scientific career
FieldsChemistry
InstitutionsUniversity of Göttingen
Doctoral advisorHeinrich Limpricht and Friedrich Wöhler
Doctoral studentsIra Remsen

Career

Fittig studied chemistry at the University of Göttingen, graduating as Ph.D. with a dissertation on acetone in 1858, under the supervision of Heinrich Limpricht and Friedrich Wöhler. He subsequently held several appointments at Göttingen, becoming Wöhler's assistant in 1858, privatdozent in 1860 and extraordinary professor in 1870. In 1870 he was appointed full professor at University of Tübingen and in 1876 at Strassburg, where the laboratories were erected from his designs.[1][2]

Fittig's research covered wide areas of organic chemistry. The aldehydes and ketones provided material for his earlier work. He observed that aldehydes and ketones may suffer reduction in neutral, alkaline, and sometimes acid solution to secondary and tertiary glycols, substances which he named pinacones; and also that certain pinacones when distilled with dilute sulfuric acid gave compounds, which he named pinacolines. The unsaturated acids also received much attention, and he discovered the internal anhydrides of oxyacids, termed lactones. He also discovered what is now known as the pinacol rearrangement, whereby 1,2-diols rearrange to aldehydes or ketones under acid catalysis.[3][4] His work involved the preparation of 2,3-dimethyl-2,3-butanediol (pinacol) from acetone,[5] followed by the rearrangement to 3,3-dimethylbutanone (pinacolone), which was then oxidised with dichromate to trimethylacetic acid.[6] Fittig's interpretation of his results was incorrect[4] and the products formed were not identified until more than a decade later when Aleksandr Butlerov independently prepared trimethylacetic acid and confirmed it was the same product as Fittig had prepared.[7]

In 1855, Charles-Adolphe Wurtz showed that when sodium acted upon alkyl iodides, the alkyl residues combined to form more complex hydrocarbons;[8][9] Fittig developed this Wurtz reaction[10][11] method by showing that a mixture of an aryl halide and an alkyl halide, under similar treatment, yielded homologues of benzene.[12][13] This process is now known as the Wurtz-Fittig reaction.[14]

His investigations on Perkin's reaction led him to an explanation of its mechanism which appeared to be more in accordance with the facts. The question, however, is one of much difficulty, and the exact course of the reaction appears to await solution. These researches incidentally solved the constitution of coumarin, the odoriferous principle of woodruff. Fittig and Erdmann's observation that γ-phenyl structural analog of isocrotonic acid readily yielded α-naphthol by loss of water was of much importance, since it afforded valuable evidence as to the constitution of naphthalene.[15] They also investigated certain hydrocarbons occurring in the high boiling point fraction of the coal tar distillate and solved the constitution of phenanthrene. We also owe much of our knowledge of the alkaloid piperine to Fittig, who in collaboration with Ira Remsen established its constitution in 1871.[1]

Fittig has published two widely used textbooks; be edited several editions of Wohler's Grundriss der organischen Chemie (11th ed., 1887) and wrote an Unorganische Chemie (1st ed., 1872; 3rd, 1882). His researches have been recognized by many scientific societies and institutions, the Royal Society awarding him the Davy medal in 1906.[1]

Notes
  1. Otto N. Witt (1911). "Obituary notices: Friedrich Konrad Beilstein, 1838–1906; Emil Erlenmeyer, 1825–1909; Rudolph Fittig, 1835–1910; Hans Heinrich Landolt, 1831–1910; Nikolai Alexandrovitsch Menschutkin, 1842–1907; Sir Walter Palmer, Bart., 1858–1910". J. Chem. Soc., Trans. 99: 1646–1668. doi:10.1039/CT9119901646.
  2. Gilman, D. C.; Peck, H. T.; Colby, F. M., eds. (1905). "Fittig, Rudolf" . New International Encyclopedia (1st ed.). New York: Dodd, Mead.
  3. Hassner, Alfred; Namboothiri, Irishi (2012). "FITTIG Pinacolone Rearrangement". Organic Syntheses Based on Name Reactions: A Practical Guide to 750 Transformations (3rd ed.). Elsevier. pp. 158–159. ISBN 9780080966304.
  4. Berson, Jerome A. (2002). "What Is a Discovery? Carbon Skeletal Rearrangements as Counter-Examples to the Rule of Minimal Structural Change". Angewandte Chemie International Edition. 41 (24): 4655–4660. doi:10.1002/anie.200290007. PMID 12481317.
  5. Fittig, R. (1859). "Ueber einige Metamorphosen des Acetons der Essigsäure" [About some metamorphoses of the acetone of acetic acid] (PDF). Justus Liebigs Annalen der Chemie (in German). 110 (1): 23–45. doi:10.1002/jlac.18591100104.
  6. Fittig, R. (1860). "Über einige Derivate des Acetons" [About some derivatives of acetone]. Justus Liebigs Annalen der Chemie (in German). 114 (1): 54–63. doi:10.1002/jlac.18601140107.
  7. Butlerov, Aleksandr (1873). "Ueber Trimethylessigsäure" [About trimethylacetic acid]. Justus Liebigs Annalen der Chemie (in German). 170 (1–2): 151–162. doi:10.1002/jlac.18731700114.
  8. Wurtz, Adolphe (1855). "Sur une Nouvelle Classe de Radicaux Organiques" [On a New Class of Organic Radicals]. Annales de Chimie et de Physique (in French). 44: 275–312.
  9. Wurtz, A. (1855). "Ueber eine neue Klasse organischer Radicale" [About a new class of organic radicals]. Justus Liebigs Annalen der Chemie (in German). 96 (3): 364–375. doi:10.1002/jlac.18550960310.
  10. "Wurtz Synthesis (Wurtz Reaction, Wurtz Reductive Coupling)". Comprehensive Organic Name Reactions and Reagents. 685: 3094–3099. 2010. doi:10.1002/9780470638859.conrr685.
  11. Kantchev, Eric Asssen B.; Organ, Michael G. (2014). "48.1.2.4 Method 4: Reductive Coupling of Alkyl Halides". In Hiemstra, H. (ed.). Alkanes. Science of Synthesis: Houben-Weyl Methods of Molecular Transformations. 48. Georg Thieme Verlag. ISBN 9783131784810.
  12. Tollens, Bernhard; Fittig, Rudolph (1864). "Ueber die Synthese der Kohlenwasserstoffe der Benzolreihe" [On the synthesis of the hydrocarbons of the benzene series]. Justus Liebigs Annalen der Chemie (in German). 131 (3): 303–323. doi:10.1002/jlac.18641310307.
  13. Fittig, Rudolph; König, Joseph (1867). "Ueber das Aethyl- und Diäthylbenzol" [About ethyl- and diethylbenzene]. Justus Liebigs Annalen der Chemie (in German). 144 (3): 277–294. doi:10.1002/jlac.18671440308.
  14. "Wurtz-Fittig Reaction". Comprehensive Organic Name Reactions and Reagents. 686: 3100–3104. 2010. doi:10.1002/9780470638859.conrr686. ISBN 9780470638859.
  15. Fittig, Rudolph; Erdmann, Hugo (1883). "Synthese des α-Naphtols" [Synthesis of α-Naphtol]. Ber. Dtsch. Chem. Ges. (in German). 16 (1): 43–44. doi:10.1002/cber.18830160115.
gollark: It's not an example, this seems to be true in all cases.
gollark: Oh, they said they don't need to be different, so square numbers are fine I guess.
gollark: I mean, you know it has 2 as a factor, and you know it divided by 2 isn't prime, implying it must have multiple prime factors (actually, *is* that the case given square numbers' existence? hmmm.)
gollark: Well, if 0 = 1 then obviously 2 = 3.
gollark: There isn't one unique answer there.

References
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