Skip to main content

Advertisement

Log in

Two-Step Preparation of Benzylacetone

  • Original Paper
  • Published:
Topics in Catalysis Aims and scope Submit manuscript

Abstract

Two-step preparation of benzylacetone has been investigated using layered double hydroxides (LDHs) as catalysts for aldol condensation of benzaldehyde and acetone and Ni supported catalysts for consecutive hydrogenation of benzylideneacetone. Activity and selectivity of LDHs of various Mg/Al ratios to desired product, benzylideneacetone, have been compared in the liquid phase at 333 K. An aldol condensation yield at 100 % conversion of benzaldehyde was 78 % using catalyst HT-2.0. In the following, optimal hydrogenation conditions—temperature of 353 K, hydrogen pressure of 5 MPa and 5 wt% of catalyst NiSAT® 320 were found. At 95 % conversion of benzylideneacetone the selectivity to desired product was 99 %.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  1. Sharma SK, Parikh PA, Jasra RV (2007) J Mol Catal A 278(1–2):135

    CAS  Google Scholar 

  2. Kunde LB, Gade SM, Kalyani VS, Gupte SP (2009) Catal Commun 10(14):1881

    Article  CAS  Google Scholar 

  3. Li F, Duan X (2006) Struct Bond 119:193

    Article  CAS  Google Scholar 

  4. Guida A, Lhouty MH, Tichit D, Figueras F, Geneste P (1997) Appl Catal A 164:251

    Article  CAS  Google Scholar 

  5. Rao KK, Gravelle M, Valente JS, Figueras F (1998) J Catal 173(1):115

    Article  CAS  Google Scholar 

  6. Lopéz J, Valente JS, Clacens J-M, Figueras F (2002) J Catal 208(1):30

    Article  Google Scholar 

  7. Campanati M, Franceschini S, Piccolo O, Vaccari A, Ziemanis A (2004) Catal Commun 5:145

    Article  CAS  Google Scholar 

  8. Szydlowska I, Beldowicz M, Malasiewicz A, Jaroszewska M, Brud WS (1987) Parf Kosmetik 68(3):137

    CAS  Google Scholar 

  9. Sokolskii DV, Erzhanov AI (1953) Doklady Akademii Nauk SSSR 93:503

    CAS  Google Scholar 

  10. Spogliarich R, Farnetti E, Kašpar J, Graziani M, Cesarotti E (1989) J Mol Catal 50(1):19

    Article  CAS  Google Scholar 

  11. Esteruelas MA, Herrero J, Lopez AM, Oro LA, Schulz M, Werner H (1992) Inorg Chem 31(19):4013

    Article  CAS  Google Scholar 

  12. Lopez-Linares F, Fuentes A, Tenia R, Martinez M, Karam A (2007) React Kinet Catal Lett 92(2):285

    Article  CAS  Google Scholar 

  13. Hu J, Chen H, Wang X, Li X, Tin K, Wang N (1998) Cuihua Xuebao 19(3):280

    CAS  Google Scholar 

  14. Bianchini C, Frediani M, Montovani G, Vizza F (2001) Organometallics 20(13):2660

    Article  CAS  Google Scholar 

  15. Burk MJ, Harper TGP, Lee JR, Kalberg C (1994) Tetrahedron Lett 35(28):4963

    Article  CAS  Google Scholar 

  16. Tabuani D, Monticelli O, Chincarini A, Bianchini C, Vizza F, Moneti S, Russo S (2003) Macromolecules 36(12):4294

    Article  CAS  Google Scholar 

  17. Callis NM, Thiery E, Le Bras J, Muzart J (2007) Tetrahedron Lett 48(46):8128

    Article  CAS  Google Scholar 

  18. Muhammad O, Sonavane SU, Sasson Y, Chidambaram M (2008) Catal Lett 125(1–2):46

    Article  CAS  Google Scholar 

  19. Kuhn W, Funk HU, Senft G (2002) WO 2002020450, assigned to Haarmann & Reimer G.M.B.H, Germany

  20. Sokolskaya AM, Ryabinina SA (1965) Vestnik Akademii Nauk Kazakhskoi SSR 21(8):45

    CAS  Google Scholar 

  21. Cornubert R, Phelisse J (1948) Comt Rend 227:1131

    CAS  Google Scholar 

  22. Kantam ML, Prakash BV, Reddy CV (2005) Synth Commun 35(14):1971

    Article  CAS  Google Scholar 

  23. Naka H, Kaneda Y, Kurata T (2001) J Oleo Sci 50(10):813

    Article  CAS  Google Scholar 

  24. Svačina P (2010) Diploma thesis. ICT, Prague

    Google Scholar 

  25. Zikmund M, Hrnčiarová K (1997) Chem Listy 91:169

    CAS  Google Scholar 

Download references

Acknowledgments

The financial support from the Ministry of Education, Youth and Sports of the Czech Republic by the research project # MSM 604 613 73 01 is gratefully acknowledged. LDHs catalysts were prepared, in kindly cooperation with Department of Solid State Engineering, ICT Prague. Süd-Chemie AG is gratefully acknowledged for providing the catalysts.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Iva Paterová.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Paterová, I., Vyskočilová, E. & Červený, L. Two-Step Preparation of Benzylacetone. Top Catal 55, 873–879 (2012). https://doi.org/10.1007/s11244-012-9853-8

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11244-012-9853-8

Keywords

Navigation