Zeolite catalyzed electrophilic substitution reaction of indoles with aldehydes: synthesis of bis (indolyl) methanes

M Karthik, AK Tripathi, NM Gupta… - Catalysis …, 2004 - Elsevier
M Karthik, AK Tripathi, NM Gupta, M Palanichamy, V Murugesan
Catalysis Communications, 2004Elsevier
Zeolites were found to catalyze electrophilic substitution reaction of indole with a variety of
aromatic aldehydes affording good to excellent yields of bis (indolyl) methanes at room
temperature. Zeolites such as Hβ, HY and H-ZSM-5 were used as catalysts to assess their
catalytic activities in the syntheses of bis (indolyl) methanes. Zn2+ ion-exchanged Y zeolite
showed better activity than parent zeolite owing to its higher Lewis acidity. The yield of bis
(indolyl) methanes increased in the following order H-ZSM-5< Hβ< HY< ZnY. Presumably …
Zeolites were found to catalyze electrophilic substitution reaction of indole with a variety of aromatic aldehydes affording good to excellent yields of bis(indolyl)methanes at room temperature. Zeolites such as Hβ, HY and H-ZSM-5 were used as catalysts to assess their catalytic activities in the syntheses of bis(indolyl)methanes. Zn2+ ion-exchanged Y zeolite showed better activity than parent zeolite owing to its higher Lewis acidity. The yield of bis(indolyl)methanes increased in the following order H-ZSM-5<Hβ<HY<ZnY. Presumably the reaction occurs at the outer zeolite surface. The catalyst is readily recyclable and reusable by a simple separation method.
Elsevier
以上显示的是最相近的搜索结果。 查看全部搜索结果