10484-56-7Relevant articles and documents
Bradshaw et al.
, p. 2051 (1972)
An efficient lutidine-assisted etherification of phenols with alkyl chloride in water
Aki, Shinji,Nishi, Takao,Minamikawa, Jun-Ichi
, p. 940 - 941 (2004)
An efficient etherification of phenol derivatives with alkyl chloride in water was achieved. The reactivity of the ether bond forming reaction was activated by addition of 2,6-lutidine.
Iron-catalyzed olefin hydrogenation at 1 bar H2 with a FeCl3-LiAlH4 catalyst
Gieshoff, Tim N.,Villa, Matteo,Welther, Alice,Plois, Markus,Chakraborty, Uttam,Wolf, Robert,Jacobi Von Wangelin, Axel
supporting information, p. 1408 - 1413 (2015/03/18)
The scope and mechanism of a practical protocol for the iron-catalyzed hydrogenation of alkenes and alkynes at 1 bar H2 pressure were studied. The catalyst is formed from cheap chemicals (5 mol% FeCl3-LiAlH4, THF). A homogeneous mechanism operates at early stages of the reaction while active nanoparticles form upon ageing of the catalyst solution. This journal is
O-Alkylation of phenol derivatives via a nucleophilic substitution
Cazorla, Clement,Pfordt, Emilie,Duclos, Marie-Christine,Metay, Estelle,Lemaire, Marc
experimental part, p. 2482 - 2488 (2011/10/31)
The alkylation of phenol derivatives can be achieved in good yield via Lewis or Bronsted acid. The only by-product of the reaction is water and the catalyst can be recycled when using Bronsted acid.
