Synlett 2015; 26(17): 2462-2466
DOI: 10.1055/s-0035-1560205
letter
© Georg Thieme Verlag Stuttgart · New York

A Facile, Convenient, and Green Route to (E)-Propenylbenzene Flavors and Fragrances by Alkene Isomerization

Casey R. Larsen
,
Erik R. Paulson
,
Gulin Erdogan
,
Douglas B. Grotjahn*
Further Information

Publication History

Received: 30 March 2015

Accepted after revision: 30 July 2015

Publication Date:
08 September 2015 (online)


This article is dedicated to Peter Vollhardt with gratitude for his creative, scientific, and mentoring influences, and his love of one-pot reactions

Abstract

(E)-Propenylbenzene flavors and fragrances can be made and isolated in high yield and selectivity by using bifunctional catalyst 1, and the heterogenized analogues. Multigram-scale reactions can be performed neat and the products isolated either by distillation, using homogeneous catalyst 1 (0.1–0.5 mol%, r.t., 10–45 min), or by decantation from heterogeneous catalysts PS-1 or PSL-1 (0.5 mol%, 70 °C, 24 h; catalyst separation and re-use shown for 3–4 cycles; 10 cycles using distilled eugenol feedstock). Both purified starting materials and essential oil feedstocks could be used. Z Isomers were present at very low levels (from 0.4% to less than 0.1%) in the products.

Supporting Information

 
  • References and Notes

  • 1 These authors contributed equally.
  • 2 Fahlbusch K.-G, Hammerschmidt F.-J, Panten J, Pickenhagen W, Schatkowski D, Bauer K, Garbe D, Surburg H. Ullmann's Encyclopedia of Industrial Chemistry . Wiley-VCH; Weinheim: 2002
  • 3 Tully TW. Flavors & Fragrances Industry Update. Tully & Holland; Wellesley (MA, USA): 2014. ; http://www.tullyandholland.com/Thpublic.asp
  • 4 Sharma SK, Srivastava VK, Jasra RV. J. Mol. Catal. A: Chem. 2006; 245: 200
  • 5 Bauer K, Garbe D, Surburg H. Common Fragrances and Flavor Materials: Preparation, Properties and Uses . Wiley-VCH; Weinheim: 1990. 2nd ed
  • 6 Chalk AJ. Flavors and Fragrances: A World Perspective . Elsevier; Amsterdam: 1988
  • 7 Leung AY. Encyclopedia of Common Natural Ingredients used in Food, Drugs and Cosmetics. Wiley; New York: 1980
  • 8 Eirew GH. US 2009035229, 2009
  • 9 Fujita K.-I, Fujita T, Kubo I. Phytother. Res. 2007; 21: 47
  • 10 Enan E. WO 2008003007, 2008
  • 11 Kouznetsov VV, Merchan Arenas DR. Tetrahedron Lett. 2009; 50: 1546
  • 12 Barnes J, Anderson LA, Phillipson JD. Herbal Medicines . Pharmaceutical Press; London: 2007. 3rd ed
  • 13 Merchan Arenas DR, Acevedo AM, Vargas Méndez LY, Kouznetsov VV. Sci. Pharm. 2011; 79: 779
  • 14 Jirovetz L, Buchbauer G, Stoilova I, Stoyanova A, Krastanov A, Schmidt E. J. Agric. Food Chem. 2006; 54: 6303
  • 15 Mallavarapu Ramesh S, Chandrasekhara RS, Rao BR. P, Kaul PN, Bhattacharya AK. Flav. Fragr. J. 1995; 10: 239
  • 16 Takeyoshi M, Iida K, Suzuki K, Yamazaki S. J. Appl. Toxicol. 2008; 28: 530
  • 17 Hua D, Ma C, Lin S, Song L, Deng Z, Maomy Z, Zhang Z, Yu B, Xu P. J. Biotechnol. 2007; 130: 463
  • 18 Padmakumari KP, Sasidharan I, Sreekumar MM. Nat. Prod. Res. 2011; 25: 152
  • 19 Findik E, Ceylan M, Elmastas M. Eur. J. Med. Chem. 2011; 46: 4618
  • 20 Fajemiroye JO, Galdino PM, De Paula JA, Rocha FF, Akanmu MA, Vanderlinde FA, Zjawiony JK, Costa EA. Food Funct. 2014; 5: 1819
  • 21 Huang Y, Ho S.-H, Lee H.-C, Yap Y.-L. J. Stored Prod. Res. 2002; 38: 403
  • 22 Zemek J, Košiková B, Augustín J, Joniak D. Folia Microbiol. 1979; 24: 483
  • 23 Cremasco MA, Braga Nd. P. Acta Amazonica 2012; 42: 275
  • 24 de Lima ME. F, Gabriel AJ. A, Castro RN. J. Braz. Chem. Soc. 2000; 11: 371
  • 25 Hartung CG, Breindl C, Tillack A, Beller M. Tetrahedron 2000; 56: 5157
  • 26 Opdyke DL. J. Monographs on Fragrance Raw Materials . Pergamon Press; Oxford: 1979
  • 27 Pines H, Stalick WM. Base Catalyzed Reactions of Hydrocarbons and Related Compounds. Academic Press; New York: 1977
  • 28 Boissier JR, Simon P, Le Bourhis B. Thérapie 1967; 22: 309
  • 29 Taylor JM, Jenner PM, Jones WI. Toxicol. Appl. Pharmacol. 1964; 6: 378
  • 30 Caujolle F, Meynier D. Acad. Sci. 1958; 246: 1465
  • 31 Miller EC, Swanson AB, Phillips DH, Fletcher TL, Liem A, Miller JA. Cancer Res. 1983; 43: 1124
  • 32 Lee HS, Lee GY. Bull. Korean Chem. Soc. 2005; 26: 461
  • 33 Rama Reddy M, Periasamy M. J. Organomet. Chem. 1995; 491: 263
  • 34 Jinesh CM, Antonyraj CA, Kannan S. Catal. Today 2009; 141: 176
  • 35 Urbala M, Krompiec S, Penkala M, Danikiewicz W, Grela M. Appl. Catal., A 2013; 451: 101
  • 36 Sharma SK, Parikh PA, Jasra RV. J. Mol. Catal. A: Chem. 2010; 317: 27
  • 37 Lastra-Barreira B, Crochet P. Green Chem. 2010; 12: 1311
  • 38 Lastra-Barreira B, Díaz-Álvarez AE, Menéndez-Rodríguez L, Crochet P. RSC Adv. 2013; 3: 19985
  • 39 Cerveny L, Krejeikova A, Marhoul A, Ruzicka V. React. Kinet. Catal. Lett. 1987; 33: 471
  • 40 Scarso A, Colladon M, Sgarbossa P, Santo C, Michelin RA, Strukul G. Organometallics 2010; 29: 1487
  • 41 Hassam M, Taher A, Arnott GE, Green IR, van Otterlo WA. L. Chem. Rev. 2015; 115: 5462
  • 42 Yu Z, Yan S, Zhang G, He W, Wang L, Li Y, Zeng F. Adv. Synth. Catal. 2006; 348: 111
  • 43 Sobczak I, Ziolek M, Pérez-Mayoral E, Blasco-Jimenéz D, Lópes-Peinado AJ, Martín-Aranda RM. Catal. Today 2012; 179: 159
  • 44 Jinesh CM, Sen A, Ganguly B, Kannan S. RSC Adv. 2012; 2: 6871
  • 45 Kishore D, Kannan S. Green Chem. 2002; 4: 607
  • 46 Luu TX. T, Lam TT, Le TN, Duus F. Molecules 2009; 14: 3411
  • 47 Menéndez-Rodríguez L, Crochet P, Cadierno V. Curr. Green Chem. 2014; 1: 128
  • 48 Gandilhon P, Charly R. DE 1936727, 1970
  • 49 Chalk AJ, Kinnelon NJ. DE 2508347, 1975
  • 50 Grotjahn DB, Larsen CR, Gustafson JL, Nair R, Sharma A. J. Am. Chem. Soc. 2007; 129: 9592
  • 51 Larsen CR. Grotjahn D. B. J. Am. Chem. Soc. 2012; 134: 10357
  • 52 Erdogan G, Grotjahn DB. J. Am. Chem. Soc. 2009; 131: 10354
  • 53 Erdogan G, Grotjahn DB. Top. Catal. 2010; 53: 1055
  • 54 Grotjahn DB, Larsen CL, Erdogan G. Top. Catal. 2014; 57: 1483
  • 55 Erdogan G, Grotjahn DB. Org. Lett. 2014; 16: 2818
  • 56 General Procedures (See Supporting Information for Details) For Table 1 Solution-Phase Experiments To substrate and internal standard in acetone-d 6 was added catalyst, and NMR integrations for reactants and products were compared with those of the standard. For Schemes 2 and 3 To air-free reactant was added solid catalyst, and aliquots were then analyzed to determine when to initiate vacuum distillation to isolate products. For Scheme 4 In a glovebox, heterogeneous catalyst was loaded into a polyethylene mesh bag that was contacted with neat reactant in a vial, using a stir bar for mixing. After 24 h, aliquots were analyzed to verify conversion. The product was squeezed out of the mesh bag and weighed, and ca. 100 mg samples were analyzed by NMR spectroscopy to determine isomeric composition. Typical Analytical Data For 5a in the mixture: 1H NMR (500 MHz, acetone-d 6): δ = 6.66 (s, 1 H), 6.33 (qd, J = 1.5, 16.0 Hz, 1 H; for the J = 1.5 Hz quartet, only the inner two peaks were fully resolved), 6.20 (qd, J = 6.5, 16.0 Hz, 1 H), 3.81 (s, 6 H), 3.71 (s, 3 H), 1.83 (dd, J = 1.5, 6.5 Hz, 3 H) ppm. 13C NMR (500 MHz, acetone-d 6): δ = 154.56, 138.72, 134.62, 132.16, 125.39, 104.37, 60.64, 56.46, 18.53 ppm. For 7a in the mixture: 1H NMR (500 MHz, acetone-d 6): δ = 7.12 (qd, J = 1.5, 12.5 Hz, 1 H), 6.88–6.95 (m, 1 H), 5.45 (qd, J = 1.5, 12.5 Hz, 1 H), 1.79–1.85 (m, 6 H), 1.63 ppm (dd, J = 1.5, 7.0 Hz, 3 H). 13C NMR (500 MHz, acetone-d 6): δ = 165.30, 139.49, 137.24, 128.56, 109.80, 14.56, 12.49, 12.09.
  • 57 Tan KH, Nishida R. J. Insect Sci. 2012; 12: 56
  • 58 Chang CL, Cho IK, Li QX. J. Econ. Entomol. 2009; 102: 203
  • 59 Kurita N, Miyaji M, Kurane R, Takahara Y. Agric. Biol. Chem. 1981; 45: 945
  • 60 Luu TX. T, Lam TT, Le TN, Duus F. Molecules 2009; 14: 3411
  • 61 Maya KM, Zachariah TJ, Krishnamoorthy B. J. Spices Aromatic Crops 2004; 13: 135
  • 62 Parthasarathy VA, Chempakam B, Zachariah TJ. Chemistry of Spices . CAB International; London: 2008
  • 63 Belanger A, Collin G, Garneau F.-X, Gagnon H, Pichette A. J. Essential Oil Res. 2010; 22: 164
  • 64 DeBaggio T, Tucker AO. The Encyclopedia of Herbs: A Comprehensive Reference to Herbs and Flavor and Fragrances. Timber Press; Portland (OR, USA): 2009
  • 65 Burdock GA. Fenaroli's Handbook of Flavor Ingredients . Taylor Francis Group; Boca Raton: 1995
  • 66 Sigma-Aldrich Product Specification: Sassafras Oil, http://www.sigmaaldrich.com/Graphics/CofAInfo/SigmaSAPQM/SPEC/W5/W510483/W510483-BULK-K_ALDRICH_.pdf.