4468-42-2Relevant articles and documents
A New Preparation Method for the Alkylation Catalysts of Aromatic Compounds Based on Immobilized AlCl3
Bykov,Belyaev
, p. 328 - 330 (2021/04/26)
Abstract: A new method for the preparation of active catalysts for the alkylation and transalkylation of aromatic compounds (benzene and toluene) based on aluminum chloride immobilized on the surface of silica gel was developed. The alkylation occurred wi
Use of Trifluoromethyl Groups for Catalytic Benzylation and Alkylation with Subsequent Hydrodefluorination
Zhu, Jiangtao,Prez, Manuel,Caputo, Christopher B.,Stephan, Douglas W.
supporting information, p. 1417 - 1421 (2016/02/14)
The electrophilic organofluorophosphonium catalyst [(C6F5)3PF][B(C6F5)4] is shown to effect benzylation or alkylation by aryl and alkyl CF3 groups with subsequent hydrodefluorination, thus resulting in a net transformation of CF3 into CH2-aryl fragments. In the case of alkyl CF3 groups, Friedel-Crafts alkylation by the difluorocarbocation proceeded without cation rearrangement, in contrast to the corresponding reactions of alkyl monofluorides.
N-Hexane activation over zeolites: Aromatic alkylation to 1-phenylhexane
Danilina, Nadiya,Payrer, Elisabeth L.,Van Bokhoven, Jeroen A.
scheme or table, p. 1509 - 1510 (2010/06/12)
Terminal 1-phenylhexane was observed during alkylation of benzene with n-hexane over 10-membered ring zeolites at moderate temperature, whereas it was not observed when 1-hexene was the reactant. The Royal Society of Chemistry 2010.