Examples of 'tert-butyl methyl ether' in a sentence
Meaning of "tert-butyl methyl ether"
Tert-butyl methyl ether (TBME) is a chemical compound commonly used as a solvent or starting material in various chemical reactions
How to use "tert-butyl methyl ether" in a sentence
Basic
Advanced
tert-butyl methyl ether
Use is preferably made of tert-butyl methyl ether.
Triturate this with tert-butyl methyl ether to afford a white solid, after collection by filtration.
The residue was extracted with tert-butyl methyl ether.
Tert-Butyl methyl ether will be preferred as ether.
Quenching was followed by extraction with tert-butyl methyl ether.
Tert-Butyl methyl ether was added to the concentrated residue, and undissolved matter was filtrated.
The most preferred antisolvent is tert-butyl methyl ether.
Tert-Butyl methyl ether is preferably used.
Especially preferred are tert-butyl methyl ether and diethyl ether.
The mixture was extracted with three portions of tert-butyl methyl ether.
The emulsion was diluted with tert-butyl methyl ether and extracted three times.
Dilution with water was followed by washing with tert-butyl methyl ether.
The solution was diluted with tert-butyl methyl ether and was extracted with ice water.
The resulting mixtures were extracted with tert-butyl methyl ether.
Tert-butyl methyl ether.
See also
This matter was thoroughly washed with tert-butyl methyl ether.
Of these, tert-butyl methyl ether gave the best results.
The obtained residue was washed with tert-butyl methyl ether.
Tert-butyl methyl ether and 2 M HCl are added to the residue.
The aqueous layer is extracted with tert-butyl methyl ether.
To this, 150 mL tert-butyl methyl ether was added and the suspension was filtered.
The combined aqueous layers were extracted with tert-butyl methyl ether.
The residue was triturated in tert-butyl methyl ether to produce the title compound ( 293 mg ).
The mixture was extracted with two portions of tert-butyl methyl ether.
Charge the tert-butyl methyl ether ( 4 I ) and blanket the flask with nitrogen.
Preferred solvents include ethers, and tert-butyl methyl ether is more preferred.
Basification with potassium carbonate was followed by extraction with tert-butyl methyl ether.
The residue was washed with tert-butyl methyl ether and filtered.
Quenching with water was followed by extraction with three portions of tert-butyl methyl ether.
To the aqueous layer was added tert-butyl methyl ether and extracted again.
The combined aqueous layers were extracted with two portions of tert-butyl methyl ether.
In the case of phenyllithium as the reagent, tert-butyl methyl ether is a particularly preferred solvent.
Dilution with water was followed by washing with two portions of tert-butyl methyl ether.
It is then diluted with water and tert-butyl methyl ether and washed with brine.
Ethanol was removed by evaporation and the residue was diluted with tert-butyl methyl ether.
Furthermore, water is soluble in tert-butyl methyl ether to the extent of only about 1 %.
The acidic aqueous layer was extracted with two portions of tert-butyl methyl ether.
The precipitation occurred and tert-butyl methyl ether ( 60 mL ) was then added.
After the completion of reaction, the mixture was diluted with tert-butyl methyl ether.
The evaporation residue is triturated with tert-butyl methyl ether ( 90 mL ) and filtered.
The reaction was quenched by the addition of further water and tert-butyl methyl ether.
The reaction is cooled to room temperature, diluted with tert-butyl methyl ether and brine.
Ethanol was removed under vacuum and the residue was diluted with tert-butyl methyl ether.
Preferably, the ether solvent is tert-butyl methyl ether.
The reaction solution is cooled and stirred with water and tert-butyl methyl ether.
Suitable solvents include water, methanol, ethanol, toluene, tert-butyl methyl ether or combinations thereof.
The reaction mixture was filtered over decalite followed by washing with tert-butyl methyl ether.
To the reaction mixture was added tert-butyl methyl ether ( 5 mL ).
After vigorously stirring for 3 h the mixture was partitioned between brine and tert-butyl methyl ether.
Examples of such solvents are acetone, methyl ethyl ketone, tert-butyl methyl ether and tetrahydrofuran.
You'll also be interested in:
Examples of using Ether
Show more
The fumes of sulphuric ether are extremely noxious
Reduces ether damage taken by a certain percentage
Commercial octabromodiphenyl ether risk management evaluation
Examples of using Methyl
Show more
Here the methyl group is not fluorinated
Laboratory and analytical uses of methyl bromide
To reducing methyl bromide consumption to no greater than
Examples of using Tert-butyl
Show more
The oxidizing agent is tert-butyl hydroperoxide
Tert-butyl alcohol is the organic complexing agent
The thiadiazole is bound to a tert-butyl group
