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Fraenkel, D., Cherniavsky, M., Ittah, B. and Levy, M. (1986) Shape-Selective Alkylation of Naphthalene and Methylnaphthalene with Methanol over H-ZSM-5 Zeolite Catalysts. Journal of Catalysis, 101, 273-283.
http://dx.doi.org/10.1016/0021-9517(86)90254-X

has been cited by the following article:

• TITLE: Improved Stability and Shape Selectivity of 2,6-Dimethylnaphthalene by Methylation of Naphthalene with Methanol on Modified Zeolites

  AUTHORS: Ye Zhang, Junpeng Feng, Zhanjun Lyu, Xuekuan Li

  KEYWORDS: Naphthalene Methylation; 2, 6-Dimethylnaphthalene; Shape-Selective; Stability; PdO Modified Zeolites

  JOURNAL NAME: Modern Research in Catalysis, Vol.3 No.2, March 18, 2014

  ABSTRACT: 2,6-Dimethylnaphthalene (2,6-DMN) is a key intermediate for polyethylene naphthalate synthesis. The selective synthesis of 2,6-DMN from naphthalene and methanol was carried out over different zeolites (HZSM-5, Hβ, HUSY and SAPO-11) modified by 0.1wt% PdO under atmospheric pressure. Among the adopted zeolites, SAPO-11 exhibits exceptional shape-selectivity and stability to synthesize 2,6-dimethylnaphthalene from methylation of naphthalene, due to the special pore structure of SAPO-11 which inosculated better with 2,6-dimethylnaphthalene than with 2,7-dimethylnaphthalene.