Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/3704
Title: Acylation of 2-methoxynaphthalene over Ion-exchanged beta zeolite
Authors: Artok, Levent
Kantarlı, İsmail Cem
Kantarlı, İsmail Cem
Izmir Institute of Technology. Chemistry
Izmir Institute of Technology. Chemistry
Issue Date: 2002
Publisher: Izmir Institute of Technology
Izmir Institute of Technology
Abstract: Friedel Crafts acylation of 2-Methoxynaphthalene was carried out over various ion-exchanged . zeolites (Mn+., where Mn+: In3+, Zn2+, Al3+, Fe3+, La3+) with various anhydride (acetic, propionic and benzoic anhydrides), or acyl chloride (acetyl, propionyl and benzoyl chlorides) acylating reagents. The results suggested that selectivity towards the 6-substituted products was higher with the larger size anhydrides, propionic and benzoic anhydrides. The metal cation type within the zeolite significantly influenced the extent of conversion and product distribution. That La3+ exchanged zeolite displayed higher selectivity for the 6-position acylated product with anhydrides ascribed mainly to narrowing of channels by the presence of La(OH)2+ ions that leave no room for the formation of more bulky isomeric forms and to enhanced Bronsted acidity of the zeolite. With acyl chlorides, the recovery of ketone products was found to be remarkably low. 1-Acyl-2-methoxynaphthalenes actively underwent deacylation when acyl chlorides were used as the acylation reagent.
Description: Thesis (Master)--Izmir Institute of Technology, Chemistry, Izmir, 2002
Includes bibliographical references (leaves: 37-40)
Text in English; Abstract: Turkish and English
vii, 40 leaves
URI: http://hdl.handle.net/11147/3704
Appears in Collections:Master Degree / Yüksek Lisans Tezleri

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