Examples of 'dimethoxyethane' in a sentence
Meaning of "dimethoxyethane"
dimethoxyethane (noun) - 'Dimethoxyethane' is a chemical compound that belongs to the class of polyethers, consisting of two methoxy (-OCH3) groups attached to an ethylene glycol chain. In English, it is predominantly utilized in organic chemistry or related fields to describe this specific compound, often in scientific research, chemical synthesis, or laboratory settings
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- The dimethyl ether of ethylene glycol; it used as a solvent
How to use "dimethoxyethane" in a sentence
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dimethoxyethane
The dimethoxyethane was removed under reduced pressure.
The solvent which is particularly preferred is dimethoxyethane.
Dimethoxyethane leads to a stronger complex than ethylene diamine.
Alternative diluents include ethers such as dimethoxyethane.
Dimethoxyethane and dimethylsulphoxide have been found to be very suitable.
Examples of the chain ether include dimethoxyethane.
Dimethoxyethane is miscible with water.
In a particular embodiment dimethoxyethane is used as solvent.
Examples of polar aprotic solvents are tetrahydrofuran and dimethoxyethane.
Suitable organic solvents are dimethoxyethane or tetrahydrofurane.
Dimethoxyethane and tetraethylene glycol dimethyl ether are particularly suitable.
The preferred method uses dimethoxyethane.
In the working examples dimethoxyethane is used as the organic complexing agent.
Inorganic salts were removed by filtration and washed with dimethoxyethane.
Dimethoxyethane is preferred.
See also
The reaction was performed in dimethoxyethane.
Dimethoxyethane is often used as a higher boiling alternative to diethyl ether and THF.
The crystallized precipitate is drained and recrystallized from boiling dimethoxyethane.
The more preferred are polyether series solvents such as dimethoxyethane and diethylene glycol dimethyl ether.
The precipitate was removed by filteration and the precipitate was washed with dimethoxyethane.
DME refers to dimethoxyethane.
The reaction is carried out preferably in a polar aprotic solvent such as tetrahydrofuran or dimethoxyethane.
Dimethoxyethane was dried over sodium-lead alloy.
The solvent used for the grafting can also be dimethoxyethane.
Dimethoxyethane is also a good solvent for oligo - and polysaccharides.
A preferred solvent is dimethoxyethane.
Preferably, THF or dimethoxyethane or solvent mixtures comprising them are used as solvent.
Among these tetrahydrofuran and the mixtures of tetrahydrofuran and dimethoxyethane are preferred.
Optimized procedures employ the dimethoxyethane complex of TiCl3 in combination with the ZnCu.
After cooling the precipitated quatemized pyridinium salt was filtered off and washed with dimethoxyethane.
The process according to claim 6 wherein dimethoxyethane is used as the polyether.
This reaction can be conducted in an appropriate solvent such as THF or dimethoxyethane.
For example, using either tetrahydrofuran or dimethoxyethane can result in a different reaction product.
In some embodiments, the solvent comprises dimethoxyethane.
Of these, dimethoxyethane and tert-butyl alcohol are most preferred.
Sulpholane ethers such as dioxane, tetrahydrofuran and dimethoxyethane.
To the warm solution was added 0.5 ml of dimethoxyethane at which point a gelatinous solid precipitated.
The non-dissolved residue was taken up in boiling dimethoxyethane.
Dimethoxyethane ( DME ) ( Aldrich, anhydrous ) was degassed vía nitrogen purge and used without further purification.
Suitable solvents include tetrahydrofuran, dimethylsulphoxide and dimethoxyethane.
Among these solvents, the use of toluene, dimethoxyethane and isopropyl acetate ( IPAC ) is more preferred.
Examples of solvents include tetrahydrofuran, dioxane, chloroform and dimethoxyethane.
NaH in DMSO or in dimethoxyethane and then with the aldehyde ( IX ).
The appropriate solvent includes tetrahydrofuran, diethyl ether or dimethoxyethane.
Dimethoxyethane ( 1.5 mL ) was added and the reaction mixture was purged three times with nitrogen / vacuum.
Preferred solvents are dioxane, tetrahydrofuran, dimethoxyethane and ethyl acetate.
Other suitable solvents include tetrahydrofuran, dimethylsulfoxide, acetone, acetaldehyde, propylene oxide, acetamide, diethylamine, and dimethoxyethane.
With solvent molecules tetrahydrofurane, dieethylether, dimethoxyethane coordinated with silicon atoms.
Examples of the solvent used in this reaction include ether, tetrahydrofuran and dimethoxyethane.
The resultant gum was partially cooled, taken up in dimethoxyethane and acidified with acetic acid.
