A. Brait et Me. Davis, Alkylation of 2-methoxynaphthalene with propylene oxide using titanium andzirconium containing molecular sieves, APP CATAL A, 204(1), 2000, pp. 117-127
Titanium and zirconium containing molecular sieves are active catalysts for
the alkylation of 2-methoxynaphthalene (2-MN) with propylene oxide (PO). T
emperatures above 423 K are necessary in order to promote the alkylation re
action. A major competing reaction that deactivates the catalyst is the oli
gomerization of PO that provides for deposition of these oligomers on the c
atalyst surface. A high 2-MN to PO ratio as well as the addition of PO in a
semi-batch mode of operation help minimize the oligomerization reaction. T
he main reaction products are an O-alkylated product (I) and four C-alkylat
ed products: 1-(2-methoxy-1-naphthyl)-2-propanol (II), 2-(2-methoxy-1-napht
hyl)propanol (III), 1-(6-methoxy-2-naphthyl)-2-propanol (IV) and 2-(6-metho
xy-2-naphthyl)propanol (V). The conversion of the limiting compound (PO) ca
n be as high as 50% with selectivities towards the desired product V rangin
g from 12 to 20%. The ratio of 2,6- to 1,2-product is 1.6 for Ti-BEA, while
Zr-BEA shows a value of 3.0. The shape-selective effect of the molecular s
ieve catalysts can be enhanced by passivation or poisoning of the outer sur
face of the catalyst by treatment with tetraethylorthosilicate (TEOS), tris
[2-(diphenylphosphino)ethyl] phosphine (TETRAPHOS-II), ethylenediaminetetr
aacetic acid (EDTA) or hydrogen peroxide (H2O2) For these cases, the 2,6- t
o 1,2-products ratios can reach values of up to 4. No leaching of Ti or Zr
from the molecular sieve materials is observed. (C) 2000 Elsevier Science B
.V. All rights reserved.