Skip to main content

Ruthenium-Catalyzed Selective Hydrogenation for Flavor and Fragrance Applications

  • Chapter
  • First Online:
Organometallics as Catalysts in the Fine Chemical Industry

Part of the book series: Topics in Organometallic Chemistry ((TOPORGAN,volume 42))

Abstract

Due to the widespread use of unsaturated alcohols as final ingredients or synthetic intermediates in the flavor and fragrance industry, there is a very high demand for safe, productive and environmentally friendly methods to access olefins with high regio and stereocontrol in addition to efficient chemoselective reduction processes of carbonyl groups in the presence of olefin moieties. These two goals were achieved by developing industrial methodologies that respectively enable regio and stereoselective 1,4-hydrogenation reactions of conjugated dienes in the presence of catalytic amounts of both cationic cyclopentadienyl-type ruthenium(II) complexes and acidic additives along with chemoselective hydrogenations of ketones and aldehydes using chloro ruthenium(II) complexes bearing amino or iminophosphines ligands as precatalysts. In this contribution, we will display few examples of such achiral transformations that could efficiently be performed on up to multi-ton scale enabling Firmenich SA to produce in a sustainable manner some ingredients such as leaf alcohol, Polysantol®, Nirvanol®, Dartanol®, or Pamplewoodol® to be used in flavor and/or fragrance applications.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Frankel EN, Selke E, Glass CA (1968) J Am Chem Soc 90:2446–2448

    Article  CAS  Google Scholar 

  2. Heinen J, Drießen-Hölscher B (1998) J Organomet Chem 570:141

    Article  Google Scholar 

  3. Steines S, Englert U, Drießen-Hölscher B (2000) J Chem Soc Chem Commun 217–218

    Google Scholar 

  4. Dupau P, Bonomo L (2008) PCT Int. Appl. WO 2008120175 A1 (Firmenich SA)

    Google Scholar 

  5. Fehr C, Magpantay I, Vuagnoux M, Dupau P (2011) Chem Eur J 17:1257–1260

    Article  CAS  Google Scholar 

  6. Ohkuma T, Ooka H, Hashiguchi S, Ikariya T, Noyori R (1995) J Am Chem Soc 117:2675–2676

    Article  CAS  Google Scholar 

  7. Okhuma T, Koizumi M, Doucet H, Pham T, Kozawa M, Murata K, Katayama E, Yokozawa T, Ikariya T, Noyori R (1998) J Am Chem Soc 120:13529–13530

    Article  Google Scholar 

  8. Cao P, Zhang X (1999) J Org Chem 64:2127–2129

    Article  CAS  Google Scholar 

  9. Okhuma T, Koizumi M, Ikehira H, Yokozawa T, Noyori R (2000) Org Lett 2:659–662

    Article  Google Scholar 

  10. Ohkuma T, Koizumi M, Yoshida M, Noyori R (2000) Org Lett 2:1749–1751

    Article  CAS  Google Scholar 

  11. Ohkuma T, Ishii D, Takeno H, Noyori R (2000) R J Am Chem Soc 122:6510

    Article  CAS  Google Scholar 

  12. Burk MJ, Hems W, Herzberg D, Malan C, Zanotti-Gerosa A (2000) Org Lett 2:4173–4176

    Article  CAS  Google Scholar 

  13. Xie J-H, Wang L-X, Fu Y, Zhu S-F, Fan B-M, Duan H-F, Zhou Q-L (2003) J Am Chem Soc 125:4404

    Article  CAS  Google Scholar 

  14. Wu J, Chen H, Kwok W, Guo R, Zhou Z, Yeung C, Chan ASC (2002) J Org Chem 67:7908–7910

    Article  CAS  Google Scholar 

  15. Henschke JP, Burk MJ, Malan C, Herzberg D, Peterson J, Wildsmith A, Cobley C, Casy G (2003) Adv Synth Catal 345:300–307

    Article  CAS  Google Scholar 

  16. Henschke JP, Zanotti-Gerosa A, Moran P, Harrison P, Mullen B, Casy G, Lennon IC (2003) Tetrahedron Lett 44:4379–4383

    Article  CAS  Google Scholar 

  17. Li W, Sun X, Zhou L, Hou G, Yu S, Zhang X (2009) J Org Chem 74:1397–1399

    Article  CAS  Google Scholar 

  18. Noyori R (2002) Angew Chem Int Ed 41:2008–2022

    Article  CAS  Google Scholar 

  19. Doucet H, Ohkuma T, Murata K, Yokozawa T, Kozawa M, Katayama E, England AF, Ikariya T, Noyori R (1998) Angew Chem Int Ed 37:1703–1707

    Article  CAS  Google Scholar 

  20. Jenck J, Germain J-E (1980) J Catal 65:133–140

    Article  CAS  Google Scholar 

  21. Noyori R, Mikami K, Ohkuma T, Terada M, Doucet H, Pham Thi Mai Trang C, Korenaga T, Ito M, Sayou N (1999) Eur Patent Appl. EP 901997 A1 (Takasago Perfumery)

    Google Scholar 

  22. Malan CG, Zanotti-Gerosa A, Henschke JP (2003) PCT Int. Appl. WO 2003048173 A1 (Chirotech Technology Ltd)

    Google Scholar 

  23. Tucker CE, Jiang Q (2003) U.S. Patent Appl. US 20030181318 A1(DSM NV).

    Google Scholar 

  24. Rautenstrauch V, Challand R, Churlaud R, Morris RH, Abdur-Rashid K, Brazi E, Mimoun H (2002) PCT Int. Appl. WO 2002022526 A2 (Firmenich SA)

    Google Scholar 

  25. Rautenstrauch V, Churlaud R, Morris RH, Abdur-Rashid K (2002) PCT Int. Appl. WO 2002040155 A1 (Firmenich SA)

    Google Scholar 

  26. Brummond KM, McCabe JM (2005) Synlett 16:2457–2460

    Article  Google Scholar 

  27. Dupau P, Bonomo L (2008) PCT Int. Appl. WO 2008120174 A1 (Innovaroma SA)

    Google Scholar 

  28. Bouachir F, Chaudret B, Dahan F, Agbossou F, Tkatchenko I (1991) Organometallics 10:455–462

    Article  CAS  Google Scholar 

  29. Mimoun H (1999) J Org Chem 64:2582–2589

    Article  CAS  Google Scholar 

  30. H. Mimoun (1999) PCT Int. Appl. 9950211 A1 (Firmenich SA)

    Google Scholar 

  31. Saudan L, Dupau P, Riedhauser J-J, Wyss Patrick P (2006) PCT Int. Appl. WO2006106483A1 (Firmenich SA)

    Google Scholar 

  32. L. Saudan, P. Dupau, J.-J. Riedhauser, P: Wyss Patrick, PCT Int. Appl. WO2006106484A1 (Firmenich SA)

    Google Scholar 

  33. Sandoval CA, Ohkuma T, Muñiz K, Noyori R (2003) J Am Chem Soc 125:13490–13503

    Article  CAS  Google Scholar 

  34. Hartmann R, Chen P (2001) Angew Chem Int Ed 40:3581–3585

    Article  CAS  Google Scholar 

  35. Abdur-Rashid K, Clapham SE, Hadzovic A, Harvey JN, Lough AJ, Morris RH (2002) J Am Chem Soc 124:15104–15118

    Article  CAS  Google Scholar 

  36. Fehr C, Vuagnoux M (2009) PCT Int. Appl. WO 2009141781 A1 (Firmenich SA)

    Google Scholar 

  37. Kraft P, Bajgrowicz JA, Denis C, Fräter G (2000) Angew Chem Int Ed 39:2980–3010

    Article  CAS  Google Scholar 

  38. Christian C, Gautier A, Blanc P-A (1995) Eur. Pat. Appl. EP 643958 A2 (Firmenich SA)

    Google Scholar 

  39. Chapuis C (2004) Chem Biodivers 1:980–102

    Article  CAS  Google Scholar 

  40. Schulte-Elte K-H, Pamingle H, Vial C (1998) Eur. Pat. Appl. EP 882697 A1 (Firmenich SA)

    Google Scholar 

  41. Yamakawa M, Ito H, Noyori R (2000) J Am Chem Soc 122:1466–1478

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Philippe Dupau .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2011 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Dupau, P. (2011). Ruthenium-Catalyzed Selective Hydrogenation for Flavor and Fragrance Applications. In: Beller, M., Blaser, HU. (eds) Organometallics as Catalysts in the Fine Chemical Industry. Topics in Organometallic Chemistry, vol 42. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3418_2011_24

Download citation

Publish with us

Policies and ethics