Examples of 'using dichloromethane' in a sentence
Meaning of "using dichloromethane"
This phrase refers to the utilization of the chemical compound dichloromethane in a particular context. It implies that the substance is being employed or applied for a specific purpose or function, which may vary depending on the given context
How to use "using dichloromethane" in a sentence
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using dichloromethane
The resulting mixture is washed using dichloromethane.
Method using dichloromethane.
The product was purified by chromatography using dichloromethane as an eluent.
The glass was transferred using dichloromethane to a conical flask and then concentrated to provide a foam.
The residue is chromatographed on silica gel using dichloromethane.
Carry out flash chromatography using dichloromethane as eluant in order to purify the resulting oil.
The residue obtained is purified on a column of silica using dichloromethane as solvent.
Chromatography using dichloromethane and methanol on silica gel afforded C185 as a solid.
The experiments were also repeated using dichloromethane as liquid medium.
The mixture is then transferred into a separating funnel and extraction is performed using dichloromethane.
The desired product is separated using dichloromethane and concentrated.
The mixture was partitioned and the aqueous layer was extracted twice using dichloromethane.
The mixture was transferred to a separatory funnel using dichloromethane and saturated aqueous sodium bicarbonate.
The organic product formed was extracted from the reaction mixture using dichloromethane.
Hazards of using Dichloromethane.
See also
It was then poured on ice and the product extracted using dichloromethane.
Chromatography on neutral alumina using dichloromethane - methanol gave the title compound, m . p.
The crude product was loaded onto the column using dichloromethane.
The reaction was carried out using dichloromethane as a co-solvent.
The reaction was stripped and applied to a silica gel column using dichloromethane.
After column chromatography on silica gel using dichloromethane as eluent, a brown solid was obtained.
The resulting organic layer is separated and aqueous layer is subjected to extraction using dichloromethane.
Concretely, the reaction is performed by using dichloromethane at room temperature.
The organic layer was separated, and the aqueous layer was subjected to extraction using dichloromethane.
The product is purified by flash chromatography, using dichloromethane with a 2.5 % acetone content as elution agent.
The reaction was filtered through a plug of celite and the celite rinsed using dichloromethane.
A series of bases was tested using dichloromethane as the solvent ( Table 6 ).
The mixture is then poured onto ice and extracted using dichloromethane.
The white residue obtained is extracted using dichloromethane ( 3 × 5 ml ) and filtered over a sintered glass.
The crude mixture was purified by chromatography on silica gel column using dichloromethane as eluent.
EXAMPLE 3 The procedure of example 2 is repeated, using dichloromethane under reflux instead of toluene.
The solution was poured over a drying column and extracted from the column using dichloromethane.
The residue is filtered over silica using dichloromethane as eluant.
The reaction is generally carried out in an inert solvent, preferably using dichloromethane.
The residue was filtered on silica gel using dichloromethane as eluent.
The oxidation reactions are carried out in an inert solvent, preferably using dichloromethane.
The residue is chromatographed on silica gel using dichloromethane as the eluent.
A saturated sodium bicarbonate solution was added to the reaction mixture, followed by extraction using dichloromethane.
The crude residue was chromatographed over silica using dichloromethane to give the title compound.
GB 2064511 discloses processes for production of cephem compounds in which acetone is extracted using dichloromethane.
The residue is purified by flash chromatography using dichloromethane as eluant.
Water was added to the residue, followed by extraction using dichloromethane.
The product is purified on a silica column using dichloromethane as solvent.
After five days, cells were harvested and menadione was extracted from the broth using dichloromethane.
The residue obtained is purified on silica using dichloromethane as eluent.
After this period, cells were harvested and menadione was extracted from the broth using dichloromethane.
The product is purified on a sigel column using dichloromethane as eluent.
Synthesis from catechol requires an additional step, Williamson ether synthesis using dichloromethane.
The product was extracted from the combined aqueous layers using dichloromethane and a continuous extractor.
For the analysis, hGH was extracted from the lipid microparticles using dichloromethane.
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The dichloromethane was evaporated under reduced pressure
The total quantity of dichloromethane loaded is unchanged
Dichloromethane and water were added to the residue
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