Abstract
The reaction of phenol and acetone to give bisphenol-A (4,4′-isopropylidenediphenol) has been investigated using zeolite as catalysts. The zeolites are less active and selective than the cation-exchange resin, Amberlyst-15.
Article PDF
Similar content being viewed by others
Avoid common mistakes on your manuscript.
References
I. Shigeru, M. Yoshio and K. Takashi, Eur. Pat. No. 319,327 (1989); Chem. Abst. 11 (1989) p194286b.
T. Nakanishi, Y. Ono, T. Miura and M. Yamazaki, Jap. Pat. No. 62,178,532 (1987) Chem. Abst. 107 (1987) p199091m.
I. Shigeru, Y. Tomitaka and M. Oshio, Jap. Pat. No. 78,741[8678,741] (1986); Chem. Abst. 105 (1986) p153678r.
S.W. Marawar and A.P. Kudchadker, Chem. Aga India 30 (1979) 411.
S. R. Guptaand M.C. Dwivedi, Chem. Age India 22. (1971) 339.
I. Shigeru, M. Yoshio and K. Takashi, Eur. Pat. No. 323,831 (1989); Chem. Abst. 112 (1990) p20776p.
C.V. Hedges and V. Mark, Aust. Pat. No. 523,293 (1982) Chem. Abst. 98 (1983) p90073b.
A.V. Bondarenko, V.G. Yaskina, V.A. Prozorov, G.G. Kryukova and V.I. Yulima, USSR Pat. No. 956,447 (1982) Chem. Abst. 98 (1983) P4383x.
Y. Setsuo, I. Yuzuru and S. Yoshio, Jap. Pat. 88/194,628 (1988) Chem. Abst. 113 (1990) p24665y.
R.J. Argauer and G.R. Landolt, US Pat. 3,702,886 (1972).
J. Paryzkova, D. Snobl and P. Matousek, Chem. Prum. 29 (1979) 30; Chem. Abst. 90 (1979) 186509j.
S. Norimitsu, Gakujutsu Kiyo-Kochi Kogyo Koto Senmon Gokko 29 (1988) 33; Chem. Abst. 1100 (1989) 231206c.
S.M. Li, US Pat. No. 4,822,923 (1989); Chem. Abst. 111 (1989) p78788t.
Q. Clayton Byerley, R. Clayton Wayne and H. William, Ger. Pat. No. 3,015,767 (1980); Chem. Abst. 94 (1981) p85087x.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Singh, A.P. Preparation of bisphenol-A over zeolite catalysts. Catal Lett 16, 431–435 (1992). https://doi.org/10.1007/BF00764901
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00764901