Synthesis of methylal from methanol and formaldehyde catalyzed by Brønsted acid ionic liquids with different alkyl groups

RSC Advances ◽  
2015 ◽  
Vol 5 (106) ◽  
pp. 87200-87205 ◽  
Author(s):  
Jiahan Sun ◽  
Hansheng Li ◽  
Haoran Song ◽  
Qin Wu ◽  
Yun Zhao ◽  
...  

The carbon chain length of ILs has an effect on its catalytic activity. The ionic liquid of [C6ImBS][HSO4] shows the best catalytic performance which is near that of concentrated sulfuric acid and p-toluene sulfonic acid.

RSC Advances ◽  
2015 ◽  
Vol 5 (71) ◽  
pp. 57968-57974 ◽  
Author(s):  
Qin Wu ◽  
Weijiao Li ◽  
Min Wang ◽  
Yu Hao ◽  
Tonghua Chu ◽  
...  

The carbon chain length of ILs has effect on its catalytic activity and [C6ImBS][HSO4]shows the best catalytic performance.


2021 ◽  
pp. 117119
Author(s):  
Mansoor Ul Hassan Shah ◽  
Ambavaram Vijaya Bhaskar Reddy ◽  
Suzana Yusup ◽  
Masahiro Goto ◽  
Muhammad Moniruzzaman

2011 ◽  
Vol 236-238 ◽  
pp. 1962-1965 ◽  
Author(s):  
Jun Min Ji

Scorbyl palmitate is a safty and highly efficient lipophilic antioxidant.It is produced by a novel ionic liquid method: L-ascorbic acid was esterified with palmitic acid to synthesize ascorbyl palmitate,using concentrated sulfuric acid as chemical catalyst in 1-Butyl-3-methy limidazolium terafluoroborate ([BMIM]BF4).The yield of ascorbyl palmitate reached 69.6±1%.


2016 ◽  
Vol 852 ◽  
pp. 485-488 ◽  
Author(s):  
Qiang Zhang ◽  
Xin Zhao ◽  
Xue Hua Zhu ◽  
Ji Hang Li

A magnetic nanoparticles supported dual acidic ionic liquid catalyst was prepared via anchoring 3-sulfobutyl-1-(3-propyltriethoxysilane) imidazolium hydrogen sulfate onto the surface of silica-coated Fe3O4 nanoparticles. And this novel supported acidic ionic liquid catalyst showed good catalytic performance in esterification. More importantly, the catalyst could be easily recovered by an external magnet and reused six times without significant loss of catalytic activity.


2019 ◽  
Vol 10 (9) ◽  
pp. 2623-2632 ◽  
Author(s):  
Melike Babucci ◽  
Chia-Yu Fang ◽  
Jorge E. Perez-Aguilar ◽  
Adam S. Hoffman ◽  
Alexey Boubnov ◽  
...  

Enveloping atomically dispersed supported iridium with the choice of ionic liquid molecular sheaths and supports controls the catalytic performance.


RSC Advances ◽  
2015 ◽  
Vol 5 (26) ◽  
pp. 19790-19798 ◽  
Author(s):  
Farhad Shirini ◽  
Omid Goli Jolodar ◽  
Mohadeseh Seddighi ◽  
Hojatollah Takbiri Borujeni

Succinimidinium hydrogensulfate ([H-Suc]HSO4), which is prepared from the reaction of succinimide and sulfuric acid, showed excellent catalytic activity for the N-Boc protection of various amines under solvent free conditions.


1988 ◽  
Vol 66 (1) ◽  
pp. 162-167 ◽  
Author(s):  
Hans Cerfontain ◽  
Ankie Koeberg-Telder

The methylation of a series of polymethylbenzenes (PoMB's) or their sulfonic acids by added hexamethylbenzene (HMB) and pentamethylbenzene-1-sulfonic acid (PeMB-1-S) as reagents in 95.5 and 98.4% H2SO4 as solvent has been studied under homogeneous conditions. HMB effects methylation of 2,4,6-trimethylbenzene-1-sulfonic acid (2,4,6-TrMB-1-S), 2,3,4,6-tetramethylbenzene-1-sulfonic acid (2,3,4,6-TeMB-1-S), and 2,3,5,6-TeMB-1-S, but not of the sulfonic acids of 1,3-dimethylbenzene (1,3-DMB), 1,2,3-TrMB, 1,2,4-TrMB, and 1,2,3,4-TeMB. PeMB-1-S is less reactive as methylating reagent than HMB. The observed substrate reactivity towards methylation by HMB was observed to decrease in the order [Formula: see text], and towards methylation by PeMB-1-S to decrease in the order [Formula: see text]. On the basis of a comparison of these orders of substrate reactivities with those predicted for the series of the PoMB-1-sulfonates and the corresponding PoMB's, it is concluded that the substrate species undergoing methylation are the PoMB's and not the corresponding sulfonates.


2004 ◽  
Vol 57 (7) ◽  
pp. 689 ◽  
Author(s):  
Zhi-Long Chen ◽  
Ronald N. Warrener ◽  
Douglas N. Butler

1,2-Bis(2,2′:6′,2′′-terpyridin-4′yl)ethanone 7, an unsymmetrically linked bis-tridentatate ligand, was prepared by treatment of 4′-cyanomethylterpyridine 10 (RT, overnight) or 4′-(methoxycarbonylmethyl)terpyridine 11 (60°C, 7 h) with concentrated hydrochloric acid. These conversions, which involved an unprecedented homo-coupling reaction, are discussed with the structure of 7 being confirmed by X-ray single crystal analysis. The nitrile starting material 10 was prepared by reaction of the mesylate 9, derived from the known 4′-hydroxymethylterpyridine 8 with sodium cyanide, while ester 11 was prepared by reaction of 10 with methanol in the presence of concentrated sulfuric acid.


1971 ◽  
Vol 49 (1) ◽  
pp. 152-156 ◽  
Author(s):  
E. Buncel ◽  
W. M. J. Strachan ◽  
H. Cerfontain

The mechanism of sulfonation of 4-hydroxyazobenzene and of 4-hydroxyazobenzene-4′-sulfonic acid in concentrated sulfuric acid media is examined through rate correlations and comparison is drawn with sulfonation of alkyl- and halogenobenzenes by means of [Formula: see text] plots. It is concluded that several mechanisms are operative in the hydroxyazobenzene system and that the curvature of the plot is the result of a change in rate-determining step from σ-complex formation to proton abstraction.


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