Examples of 'aprotic organic' in a sentence
Meaning of "aprotic organic"
aprotic organic - This phrase is typically used in chemistry to describe organic compounds that do not contain a protic hydrogen
How to use "aprotic organic" in a sentence
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aprotic organic
The aprotic organic diluent is generally inert.
Crotamiton is mentioned as suitable aprotic organic solvent.
Suitable aprotic organic solvents are hydrocarbons and ethers.
In the present process an aprotic organic diluent is used.
The aprotic organic solvent may comprise a hydrocarbon solvent.
Currently preferred polar aprotic organic solvents include acetonitrile.
The aprotic organic diluent is preferably considered generally such as a liquid solvent.
The solvent used is a weakly basic aprotic organic solvent.
Preferred of the aprotic organic diluents are the haloalkanes.
Some suitable organic solvents include aprotic organic solvent.
Preferably the aprotic organic solvent is immiscible with water.
In the present hydrocarbylation step an aprotic organic diluent is used.
The non-polar aprotic organic solvent is likewise as defined above.
In the present halogenation step an aprotic organic diluent is used.
The aprotic organic solvent may be a hydrocarbon solvent, such as hexane.
See also
Suitable solvents for the reaction are polar aprotic organic solvents.
The reaction is conducted in an aprotic organic solvent such as dichloromethane or tetrahydrofuran.
The examples illustrate the use of dimethylformamide as the aprotic organic solvent.
Convenient solvents include polar aprotic organic solvents, such as dimethylformamide.
Applicable solvents for use in the process of the invention are aprotic organic solvents.
As the aprotic organic solvent, aprotic ethers and esters are preferable.
The reactants are typically contacted in a suitable aprotic organic solvent such as tetrahydrofuran.
For this reaction, an aprotic organic solvent such as tetrahydrofuran, benzene or toluene is used.
Other examples of the first solvent also include aprotic organic solvents.
Polar or non-polar aprotic organic solvents may be mentioned as suitable solvents.
The reactants are typically contacted in a suitable aprotic organic solvent such as toluene.
Preferably the solvent is an aprotic organic solvent, such as tetrahydrofuran, dimethoxyethane or a mixture thereof.
Suitable reaction media for variant b are in particular nonpolar and polar aprotic organic solvents.
Currently preferred non-polar aprotic organic solvents include dichloromethane and toluene.
Dissolving rocuronium bromide in a polar aprotic organic solvent ;.
Exemplary inert aprotic organic solvents includes carbon tetrachloride, benzene, chlorobenzene and cyclohexane.
The reactants are typically contacted in a suitable aprotic organic solvent such as dimethylformamide.
Amounts of the aprotic organic diluent thus required can, in general, vary over a wide range.
The reactants are typically contacted in a suitable aprotic organic solvent such as methylene chloride.
Preferably, aprotic organic solvents such as DMF or THF are utilized.
If the reagent is an organometallic agent, aprotic organic solvents are typically preferred.
The cyclization is preferably carried out in an organic solvent, preferably an aprotic organic solvent.
Suitable solvents for the reaction include aprotic organic solvents such as tetrahydrofuran, diethyl ether.
No purity enhancement was observed during hot ( reflux ) slurries in aprotic organic solvents.
Typical solvents are aprotic organic solvents, hence they can not take part in the reaction.
A preferred class of solvents comprises slightly polar, aprotic organic solvents.
Currently preferred polar aprotic organic solvents include acetonitrile and N, N-dimethyl acetamide.
The reaction is typically carried out in a suitable aprotic organic solvent, e . g.
In one embodiment, the aprotic organic solvent is di-n-propyl ether.
In some embodiments of the method, the reaction is performed in an aprotic organic solvent.
Suitable solvents for sodium triacetoxyborohydride include aprotic organic solvents such as tetrahydrofuran, acetonitrile or dichloroethane.
However, an additional solvent can be present which is generally an aprotic organic solvent.
In one embodiment, the aprotic organic solvent is DCM.
The flowable composition also includes a biocompatible, polar aprotic organic liquid.
A polar aprotic organic solvent ;.
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