Abstract
Aromatic acetals were prepared by condensation of 2-methyl-3-(4-R-phenyl)propanals (R = Me, i-Pr, i-Bu) with ethanol, methanol, ethylene glycol, 1,2-propanediol, methyl Cellosolve, and Cellosolve. The perfume characteristics of the acetals were studied.
Similar content being viewed by others
REFERENCES
Ohloff, G., Helv. Chim. Acta, 1992, vol. 75, no. 7, pp. 2041-2108.
Weyerstahl, P. and Brendel, J., Lieb. Ann., 1990, no. 10, pp. 1029-1036.
Tadeba, H. and Mihara, S. Agr. Biol. Chem., 1990, vol. 54, no. 9, pp. 2271-2276.
Buchbauer, G., Spreitzer, H., and Kotlan, U., Z. Naturforsch. (b), 1991, vol. 46, no. 9, pp. 1272-1274.
Voitkevich, S.A., 865 dushistykh veshchestv dlya parfyumerii i bytovoi khimii (865 Fragrants for Perfumery and Domestic Chemicals), Moscow: Pishchevaya Prom—st., 1994.
Polyanskii, N.G., Kataliz ionitami talysis with Ion Exchangers) Moscow: Khimiya, 1973.
Voitkevich, S.A. and Kheifets, A.A., Ot drevnikh blagovonii k sovremennym parfyumerii i kosmetike From Ancient Fragrances to Modern Perfumes and Cosmetics), Moscow: Pishchevaya Prom—st., 1997.
Burkert, U. and Allinger, N.L., Molecular Mechanics, Washington, DC: Am. Chem. Soc., 1982.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Vyglazov, O.G., Chuiko, V.A., Izotova, L.V. et al. Synthesis and Perfume Characteristics of Acetals Containing an Aromatic Ring. Russian Journal of Applied Chemistry 74, 1888–1891 (2001). https://doi.org/10.1023/A:1014848929083
Issue Date:
DOI: https://doi.org/10.1023/A:1014848929083