Examples of 'aprotic solvents' in a sentence
Meaning of "aprotic solvents"
Aprotic solvents are types of solvents that do not have available protons (H+ ions) or hydrogen-bonding capabilities. These solvents are used in various chemical processes, such as inorganic reactions, synthesis of pharmaceuticals, and polymer chemistry. Aprotic solvents are known for their ability to dissolve a wide range of substances and their relatively low reactivity with other chemicals. Some examples of aprotic solvents include acetone, dimethyl sulfoxide (DMSO), and hexane
How to use "aprotic solvents" in a sentence
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aprotic solvents
Preferred solvents are aprotic solvents such a pyridine.
Particularly preferred volatile solvents are aprotic solvents.
Polar aprotic solvents lack an acidic hydrogen.
The organic solvents preferably are aprotic solvents.
Suitable aprotic solvents are acetonitrile and ethers.
Particularly suitable organic solvents are aprotic solvents.
Suitable aprotic solvents are those previously defined.
A preferred class of solvents is dipolar aprotic solvents.
Suitable bases and aprotic solvents are described hereinbefore.
Aprotic solvents do not adversely affect the reaction.
They can also include aprotic solvents.
Suitable aprotic solvents are as described herein.
Preferred solvents are polar aprotic solvents.
Examples of polar aprotic solvents are tetrahydrofuran and dimethoxyethane.
Certain adjuvants can also be polar aprotic solvents.
See also
A mixture of polar aprotic solvents may also be used.
It is also possible to use mixtures of these aprotic solvents.
In general aprotic solvents are found to damage biological molecules.
The reaction is performed in aprotic solvents.
Suitable aprotic solvents are as described above.
Suitable inert solvents include dipolar aprotic solvents.
Examples of aprotic solvents are given above.
Preferred solvents are protic or aprotic solvents.
Preferred aprotic solvents include toluene and xylenes.
Superoxide can also be generated in aprotic solvents by cyclic voltammetry.
Certain aprotic solvents are polar solvents.
Suitable cosolvents include the aprotic solvents mentioned herein.
Aprotic solvents are used as reaction solvents in the present invention.
Suitable solvents include aprotic solvents such as toluene.
Aprotic solvents are preferable to protic solvents during the hydrogenation.
Suitable solvents are dipolar aprotic solvents such as dimethylfomamide.
These aprotic solvents can be used either individually or in combination.
Suitable solvents are polar aprotic solvents such as tetrahydrofuran.
The adducts have an increased solubility in polar aprotic solvents.
Preferably aprotic solvents are used.
The solvent medium should be selected from aprotic solvents.
Preferred aprotic solvents are ketones.
It is of course also possible to use mixtures of these aprotic solvents.
The reaction is typically run in aprotic solvents at elevated temperature.
Polar aprotic solvents are solvents that lack an acidic hydrogen.
Preferred organic solvents are ethers or aprotic solvents such as toluene.
The use of polar aprotic solvents is preferred among these solvents.
The reaction thus has to be carried out in aprotic solvents.
The abovementioned polar aprotic solvents can be used in this reaction.
Aprotic solvents such as dichloromethane or toluene are preferred for this transformation.
Adjuvants as polar aprotic solvents.
The use of aprotic solvents such as diglyme for example is advantageous.
Preferred solvents are esters and dipolar aprotic solvents as described above.
Polar aprotic solvents which can be utilized include ether solvents.
Of course also mixtures of protic and aprotic solvents may be used.
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Examples of using Aprotic
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In an aprotic solvent and in the presence of a base
Preferred solvents are aprotic solvents such a pyridine
An aprotic polar solvent is preferable as the solvent
Examples of using Solvents
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Do not use solvents or other aggressive or abrasive
Do not use harsh or abrasive cleaners or solvents
Do not use solvents or immerse the product
