scholarly journals Renewable Dimethyl Carbonate for Tertiary Amine Quaternisation: Kinetic Measurements and Process Optimisation

Author(s):  
Roel Jacob Thomas Kleijwegt ◽  
Vera C. Henricks ◽  
Wyatt Winkenwerder ◽  
Wim Baan ◽  
John van der Schaaf

Quaternary ammonium salts (QAS) are an important part of the increasing surfactant market. Conventional production processes employ toxic alkyl halides in a Menshutkin reaction with a tertiary amine (DMDA). Dimethyl...

Polymer ◽  
1996 ◽  
Vol 37 (7) ◽  
pp. 1267-1271 ◽  
Author(s):  
Philip Hodge ◽  
Richard O'Dell ◽  
Michael S.K. Lee ◽  
John R. Ebdon

2017 ◽  
Vol 2017 ◽  
pp. 1-6
Author(s):  
Carlos A. González-González ◽  
Juan Javier Mejía Vega ◽  
Ricardo García Monroy ◽  
Davir González-Calderón ◽  
David Corona-Becerril ◽  
...  

The process ofN-alkylation of several pyrroles, indoles, and derivative heterocycles is herein described, using quaternary ammonium salts as the source of an alkylating agent. These reactions were carried out on several heterocyclic rings with triethylbenzylammonium chloride or tetradecyltrimethylammonium bromide and an NaOH solution at 50%, leading to a chemoselectiveN-alkylated product and an average yield of 73%. This is an alternative process to the traditional benzylation and methylation ofN-heterocycles with direct handling of alkyl halides.


Synthesis ◽  
2017 ◽  
Vol 49 (16) ◽  
pp. 3535-3545 ◽  
Author(s):  
Charles Diesendruck ◽  
Shlomy Arava

The N-arylation of tertiary amines to provide sp3 quaternary ammonium salts is a challenge in organic chemistry. To date, no general method for such arylations has been established. Here, we summarize a variety of strategies that have been tested, starting with harsh nucleophilic aromatic substitutions, through to the use of copper catalysis and the application of strong electrophiles, such as phenyl cations and benzynes. The achievements and limitations of each method are summarized, and the challenges yet to be met in the synthesis of charged ammonium compounds are described.1 Introduction2 Alkylation of Anilines: The Menshutkin Reaction3 Arylations3.1 Nucleophilic Aromatic Substitutions by Tertiary Amines3.2 Preparation of N-Arylpyridinum Salts from Zincke and Pyrylium Salts3.3 Arylations Using Phenyl Cations3.4 Copper-Catalyzed Arylation of N-Heteroarenes3.5 Benzynes as Aryl Electrophiles4 Conclusions and Perspective


2008 ◽  
Vol 2 (2) ◽  
pp. 147-152
Author(s):  
Sergey Nikulin ◽  
◽  
Viacheslav Misin ◽  

In the review physical and chemical aspects and technological parameters of the rubbers production processes from industrial latex with application of ammonium halogenides, tetraalkylammonium salts, poly-(N,N-dimethyl-2-oxypropyleneammonium) chloride, poly-N,N-dimethyl-N,N-diallylammonium chloride, and his copolymer with SO2 are considered. A significant ecological effect of polymeric flocculants application is shown.


Talanta ◽  
1996 ◽  
Vol 43 (11) ◽  
pp. 1931-1939 ◽  
Author(s):  
F MOHAMED ◽  
A MOHAMED ◽  
H MOHAMED ◽  
S HUSSEIN

Author(s):  
Tomasz K. Olszewski ◽  
Anna Brol

An effective protocol for quaternization of simple 1-aminoalkylphosphonic acids under basic conditions and using Me2SO4 as convenient alkylating agent is reported. In the course of reaction phosphonic acid quaternary ammonium...


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