Examples of 'tert-butyl methyl' in a sentence
Meaning of "tert-butyl methyl"
tert-butyl methyl: This phrase refers to a chemical compound composed of a methyl group (CH3) attached to a tert-butyl group. It is commonly used in organic chemistry, particularly in the synthesis of various organic compounds and pharmaceuticals
How to use "tert-butyl methyl" in a sentence
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tert-butyl methyl
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.
Crystallization from tert-butyl methyl ether / hexane affords the title compound as white crystals.
Quenching was followed by extraction with tert-butyl methyl ether.
Upon addition of the tert-butyl methyl ether, solids precipitated out of the reaction mixture.
The most preferred antisolvent is tert-butyl methyl ether.
After dilution with tert-butyl methyl ether, the reaction mixture was successively washed with a sat.
This matter was thoroughly washed with tert-butyl methyl ether.
Tert-Butyl methyl ether will be preferred as ether.
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.
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The resulting mixtures were extracted with tert-butyl methyl ether.
Tert-Butyl methyl ether was added to the concentrated residue, and undissolved matter was filtrated.
The obtained residue was washed with tert-butyl methyl ether.
Tert-Butyl methyl ether is preferably used.
The aqueous layer is extracted with tert-butyl methyl ether.
Tert-butyl methyl ether.
The residue was washed with tert-butyl methyl ether and filtered.
Basification with potassium carbonate was followed by extraction with tert-butyl methyl ether.
To the aqueous layer was added tert-butyl methyl ether and extracted again.
Quenching with water was followed by extraction with three portions of tert-butyl methyl ether.
In the case of phenyllithium as the reagent, tert-butyl methyl ether is a particularly preferred solvent.
The combined aqueous layers were extracted with two portions of tert-butyl methyl ether.
It is then diluted with water and tert-butyl methyl ether and washed with brine.
Dilution with water was followed by washing with two portions of tert-butyl methyl ether.
Of these, tert-butyl methyl ether gave the best results.
The combined aqueous layers were extracted with tert-butyl methyl ether.
Preferred solvents are tert-butyl methyl ether, isopropyl alcohol, toluene, heptane, dichloromethane and the like.
The mixture was extracted with two portions of tert-butyl methyl ether.
The preferred ether is selected from tert-butyl methyl ether, tetrahydrofuran, diisopropyl ether, and diethyl ether.
The acidic aqueous layer was extracted with two portions of tert-butyl methyl ether.
Furthermore, water is soluble in tert-butyl methyl ether to the extent of only about 1 %.
Ethanol was removed by evaporation and the residue was diluted with tert-butyl methyl ether.
Tert-butyl methyl ether and 2 M HCl are added to the residue.
Preferred solvents include ethers, and tert-butyl methyl ether is more preferred.
Charge the tert-butyl methyl ether ( 4 I ) and blanket the flask with nitrogen.
The reaction mixture was heated to distill the tert-butyl methyl ether / water azeotrope.
To this, 150 mL tert-butyl methyl ether was added and the suspension was filtered.
After the completion of reaction, the mixture was diluted with tert-butyl methyl ether.
The precipitation occurred and tert-butyl methyl ether ( 60 mL ) was then added.
The reaction was quenched by the addition of further water and tert-butyl methyl ether.
The residue was triturated in tert-butyl methyl ether to produce the title compound ( 293 mg ).
Ethanol was removed under vacuum and the residue was diluted with tert-butyl methyl ether.
The suitable solvent is tert-butyl methyl ether ; and the compound of formula ( IV ) is,.
The reaction is cooled to room temperature, diluted with tert-butyl methyl ether and brine.
The resulting oil was treated with boiling tert-butyl methyl ether, and a precipitate formed.
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Examples of using Tert-butyl
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The oxidizing agent is tert-butyl hydroperoxide
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The thiadiazole is bound to a tert-butyl group
