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Butyl-methylimidazolium

ENIM]C1 AICI31 [BP] Cl AICI3 J [BMIM] = 1-butyl-3-methylimidazolium cation [EMIM] = l-ethyl-3-methylimidazolium cation [BP] = N-l-butylpyridinium cation... [Pg.279]

We recently prepared various types of differently fiuorinated alkyl sulfate ILs and discovered that the hydrophobicity was dependent on the content ratio of the fluorine on the alkyl sulfate anion and 2,2,3,3,4,4,5,5-octafiuoropentyl sulfate salts showed hydrophobic properties. Melting point and viscosity were also dependent on the fluorine contents of the anionic part, while conductivity was determined by the cationic part and not influenced by the fluorine contents. Efficient lipase-catalyzed transesterificafion was demonstrated using hydrophobic 1-butyl-3-methylimidazolium 2,2,3,3,4,4,5,5-octafiuoropentyl sulfate ([bmim][C5E8]) as solvent (Eig. 6). ... [Pg.9]

Table 4.2 Effect of the anion on the melting point of the 1 -butyl-3-methylimidazolium, [bmim]+, cation... Table 4.2 Effect of the anion on the melting point of the 1 -butyl-3-methylimidazolium, [bmim]+, cation...
The experimental simplicity of Method 3 has attracted the specialists in modern trends in catalysis. Thus, in Method 3 different authors used RbF (04SC4431), MgO (09EJM3805), KF/AI2O3, mixed magnesium-aluminum carbonate, or mixed magnesium-lanthanum oxide (08TL2730) in methanol. Recently, 2-aminopyran syntheses with acetylacetone 35 and ethyl acetoacetate 36 were carried out in an ionic liquid [(bmim)(BF4), 1-butyl-3-methylimidazolium borofluoride] with 1,1,3,3-tetramethylguanidine as... [Pg.199]

C. 1- Butyl-3-methylimidazolium hexafluorophosphate. A 1-L, one-necked, round-bottomed flask (Note 13) is charged with 65.6 g (0.37 mol, 1 equiv) of 1- butyl-3-methylimidazolium chloride, and 69.3 g (0.37 mol, 1 equiv) of potassium hexafluorophosphate (Note 19) in 70 ml of distilled water. The reaction mixture is stirred at room temperature for 2 hr affording a two-phase system. The organic phase is washed with 3 X 50 mL of water and dried under reduced pressure (0.1 mbar, 0.001 mm). Then 100 ml of dichloromethane and 35 g of anhydrous magnesium sulfate are added. After 1 hr, the suspension is filtered and the volatile material is removed under reduced pressure (0.1 bar, 0. 1 mm) at 30°C for 2 hr to afford 86.4 g (0.29 mol, 81%) of 1- butyl-3-methylimidazolium hexafluorophosphate as alight yellow viscous liquid, mp 10°C (Notes 20 and 21). [Pg.120]

PHYSICAL CHEMICAL PROPERTIES FOR 1-BUTYL-3-METHYLIMIDAZOLIUM BASED IONIC LIQUIDS... [Pg.122]

Butyl-3-methylimidazolium chloride IH-lmidazolium, 1-butyl-3-methyl-, chloride (10) (79917-90-1)... [Pg.269]

A new protocol was developed for the synthesis of A-substituted thioamides, employing arenes and isothiocyanates in 1-butyl-3-methylimidazolium chloro-aluminate IL, [bmim][AlCl4], as a homogenous Lewis acid catalyst and solvent,Scheme 12. [Pg.167]

The enthalpy difference befween the AA and the GA conformers in the [C4CiIm][BFJ is much smaller than the corresponding enthalpy difference befween the conformers of a free butane chain. This indicates that the 1-butyl-3-methylimidazolium cations most likely form local liquid structures specific fo each rofafional isomers [50]. Coexistence of these local structures, incorporating different rotational isomers, seems to hinder crystallization. This is probably the reason for fhe low melting points of such ILs. [Pg.335]

The Diels-Alder reaction is an important and widely used reaction in organic synthesis (Sauer and Sustmann, 1980), and in the chemical industry (Griffiths and Previdoli, 1993). Rate enhancement of this reaction has been achieved by the use of solvents such as water, surfactants, very high pressure, lithium amides, alkylammonium nitrate salts, and macrocyclic hosts (Sherman et ak, 1998). Diels-Alder reactions can be ran in neutral ionic liquids (such as 1-butyl-3-methylimidazolium trifluoromethanesulfo-nate, l-butyl-3-methylimidazolium hexafluorophophate, l-butyl-3-methylimidazolium tetrafluoroborate, and l-butyl-3-methylimidazolium lactate). Rate enhancements and selectivities are similar to those of reactions performed in lithium perchlorate-diethyl ether mixtures. [Pg.173]

A. 1-Butyl-3-methylimidazolium chloride. A 2-L, three-necked, round-bottomed flask is equipped with a heating oil bath, a nitrogen inlet adapter, an internal thermometer adapter, an overhead mechanical stirrer, and a reflux condenser. The flask is flushed with... [Pg.236]

Butyl-3-methylimidazolium tetrafluoroborate 1 H-lmidazolium, 1 -butyl-3-methyl-, tetrafluoroborate(l-) (13) (174501-65-6)... [Pg.243]

Another type of room temperature ionic liquids are typically the salts between cations like 1-butyl-3-methylimidazolium (BMI+), l-ethyl-3-methylimidazolium, and 1-butyl-pyridinium (see Scheme) and anions like BF7, PFq, CF3COO , CF3S03 and (CF3S02)2] T [29, 30]. By suitably selecting the cation and the anion, we can design ionic liquids that are nonvolatile, nonflammable, chemically stable, highly... [Pg.328]


See other pages where Butyl-methylimidazolium is mentioned: [Pg.155]    [Pg.267]    [Pg.276]    [Pg.626]    [Pg.163]    [Pg.179]    [Pg.375]    [Pg.226]    [Pg.1]    [Pg.668]    [Pg.522]    [Pg.266]    [Pg.266]    [Pg.268]    [Pg.289]    [Pg.143]    [Pg.438]    [Pg.438]    [Pg.439]    [Pg.440]    [Pg.442]    [Pg.126]    [Pg.237]    [Pg.237]    [Pg.238]    [Pg.238]    [Pg.241]    [Pg.569]    [Pg.142]   


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1 -butyl-3-methylimidazolium tetrafluoroborate [BMIm

1 -n-butyl-3-methylimidazolium

1- Butyl-3-methylimidazolium C4mim

1- Butyl-3-methylimidazolium cation

1- Butyl-3-methylimidazolium chloride

1- Butyl-3-methylimidazolium oxidation with

1- Butyl-3-methylimidazolium tetrafluoroborate

1- Butyl-3-methylimidazolium tetrafluoroborate ionic liquid[bmim

1-butyl-3-methylimidazolium [BMIM

Butyl-methylimidazolium hexafluorophosphate

Ionic liquid , l-Butyl-3-methylimidazolium tetrafluoroborate

Ionic liquids 1 -butyl-3-methylimidazolium hexafluorophosphate

Ionic liquids, l-butyl-3-methylimidazolium

Ionic liquids-assisted preparation 1 -butyl-3-methylimidazolium

L-Butyl-3-methylimidazolium bromide

L-Butyl-3-methylimidazolium cation

L-Butyl-3-methylimidazolium hexafluorophosphate ([bmim

L-Butyl-3-methylimidazolium salts

L-Butyl-3-methylimidazolium tosylate

L-Butyl-3-methylimidazolium-based ionic

L-Butyl-3-methylimidazolium-based ionic liquids

L-butyl-3-methylimidazolium

L-butyl-3-methylimidazolium [BMIM

L-butyl-3-methylimidazolium bis

L-butyl-3-methylimidazolium chloride

L-butyl-3-methylimidazolium chloride bmimCl)

L-butyl-3-methylimidazolium chloroaluminate

L-butyl-3-methylimidazolium dicyanamide

L-butyl-3-methylimidazolium hexafluorophosphate

L-butyl-3-methylimidazolium tetrafluoroborate

L-n-butyl-3-methylimidazolium [BMIM

L-n-butyl-3-methylimidazolium bromide

Methylimidazolium

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