Examples of 'aprotic organic solvents' in a sentence
Meaning of "aprotic organic solvents"
aprotic organic solvents - These are solvents that do not contain any hydrogen bonded directly to an oxygen or nitrogen atom. They are often used in chemical reactions where protic solvents would interfere or cause unwanted side reactions
How to use "aprotic organic solvents" in a sentence
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aprotic organic solvents
Suitable aprotic organic solvents are hydrocarbons and ethers.
Suitable solvents for the reaction are polar aprotic organic solvents.
Polar or non-polar aprotic organic solvents may be mentioned as suitable solvents.
Other examples of the first solvent also include aprotic organic solvents.
Currently preferred polar aprotic organic solvents include acetonitrile.
Applicable solvents for use in the process of the invention are aprotic organic solvents.
Currently preferred non-polar aprotic organic solvents include dichloromethane and toluene.
Suitable reaction media for variant b are in particular nonpolar and polar aprotic organic solvents.
Exemplary inert aprotic organic solvents includes carbon tetrachloride, benzene, chlorobenzene and cyclohexane.
If the reagent is an organometallic agent, aprotic organic solvents are typically preferred.
Examples of suitable organic solvents for embodiment ( ii ) are nonpolar and polar aprotic organic solvents.
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.
Suitable solvents for sodium triacetoxyborohydride include aprotic organic solvents such as tetrahydrofuran, acetonitrile or dichloroethane.
Solvents that can be used are dimethylformamide, dimethylacetamide, acetonitrile and like aprotic organic solvents.
See also
Preferably, aprotic organic solvents such as DMF or THF are utilized.
A preferred class of solvents comprises slightly polar, aprotic organic solvents.
Currently preferred polar aprotic organic solvents include acetonitrile and N, N-dimethyl acetamide.
Suitable solvents which may be mentioned are polar or non-polar aprotic organic solvents.
Currently preferred non-polar aprotic organic solvents include toluene, chlorobenzene, and dichloromethane.
If the reagent is a nucleophilic reagent, both protic and aprotic organic solvents may be used.
Aprotic organic solvents are, for example, ketones, ethers, esters and nitriles, without being restricted thereto.
Suitable solvents for the one-pot reaction comprise polar aprotic organic solvents.
Suitable solvents include aprotic organic solvents such as diethyl ether, dioxane, tetrahydrofuran, and the like.
Suitable solvents include aprotic solvents, including but not limited to polar aprotic organic solvents.
Some suitable organic solvents include polar aprotic organic solvents such as N, N-dimethylformamide.
Organic solvents may be, for example, polar, apolar, protic or aprotic organic solvents.
Representative examples of apolar aprotic organic solvents include toluene, xylenes, Hex, Hept, CHex and MeCHex.
Suitable solvents are aprotic organic solvents ( e.g., tetrahydrofuran, dimethylformamide, and the like ).
Suitable solvents are aprotic organic solvents such as benzene, toluene, THF, CH ₂ Cl ₂ and ethyl acetate.
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