Examples of 'dichloromethane solution' in a sentence
Meaning of "dichloromethane solution"
Dichloromethane solution refers to a liquid mixture where dichloromethane, a type of solvent, is the major component and is typically used in chemical processes or laboratory experiments
How to use "dichloromethane solution" in a sentence
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dichloromethane solution
The dichloromethane solution was concentrated to a crude oil.
The salt was precipitated by addition of the dichloromethane solution into heptane.
The dichloromethane solution was concentrated down to an oil.
The salt was precipitated by addition of the dichloromethane solution into heptanefollowed by concentration.
The dichloromethane solution was dried and evaporated.
The amount of base was then compared with a dichloromethane solution at the initial concentration.
The dichloromethane solution was concentrated to dryness as an oil.
The mixture was separated and the dichloromethane solution concentrated on a rotary evaporator.
Dichloromethane solution is dried and evaporated to dryness.
Insoluble substances were filtered off by celite to obtain a dichloromethane solution of the active ester.
The dichloromethane solution was concentrated in vacuo to give a gum.
The resin was isolated as white granules by steam precipitation from the dichloromethane solution.
This dichloromethane solution was used in the next step.
The product is stable in dry, neutral dichloromethane solution.
Dichloromethane solution was dried over anhydrous magnesium sulfate.
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The phases were separated and the dichloromethane solution used in the subsequent step below.
The dichloromethane solution was separated and washed with brine.
Following a methanol rinse, the cartridge was loaded with a dichloromethane solution of crude product.
The dichloromethane solution was concentrated.
Next, the solution was dropped with a dichloromethane solution containing Compound No.
This dichloromethane solution can be used in the next step.
Crystals were obtained by slow diffusion of methanol to a dichloromethane solution of 11 ′.
The resulting dichloromethane solution was concentrated for solvent removal.
The resin was isolated as white granules ( 95 kg ) by steam precipitation from the dichloromethane solution.
The dichloromethane solution was partially evaporated and ethyl acetate was added.
To this solution was added dropwise a 10 ml dichloromethane solution containing 1.36 ml boron tribromide.
The dichloromethane solution was then slowly poured into a stirred mixture of satd.
With stirring, to this was added dropwise 30 ml of a dichloromethane solution containing 9.97 g of boron tribromide.
Dry the dichloromethane solution with magnesium sulfate and evaporate to a foam.
Of ethyl glutarate NHS ester in dry dichloromethane solution ( 10 mL ).
The combined dichloromethane solution was evaporated to give the crude mesylate.
This transformation is best done in dichloromethane solution using dimethylcarbamoyl chloride as the activating electrophile.
A dichloromethane solution of the benzylic alcohol was treated with phosphorous tribromide at ambient temperature.
IMS ( 2 I ) was added to the dichloromethane solution and distillation started.
The dichloromethane solution is then evaporated under reduced pressure to a volume of approximately 4 vols.
The deblocking solution used was dichloromethane solution containing 3 % ( w / v ) trifluoroacetic acid.
The dichloromethane solution was concentrated and the crude oil was purified by flash chromatography.
An aliquot of the dichloromethane solution was used for the next stage.
The dichloromethane solution thus obtained is washed with water and then evaporated to dryness.
Another 5 ml of dichloromethane solution containing adipoyl chloride was added dropwise.
The dichloromethane solution was extracted from this mixture and then dried over magnesium sulphate.
The combined dichloromethane solution was concentrated by distillation collecting 1L.
The Dichloromethane solution was washed with a solution of sodium bicarbonate.
After workup a dichloromethane solution TFP ester was treated with 6-aminohexanol.
This dichloromethane solution of Id was used without isolation in the preparation of compound le.
The above-prepared dichloromethane solution was then added thereto, followed by stirring for 1 hour.
The dichloromethane solution was dried over MgSO4 and evaporated.
The above-prepared dichloromethane solution was then added thereto, followed by stirring for 30 minutes.
The dichloromethane solution was poured uniformly over about 3 hours.
The obtained dichloromethane solution was used in the next reaction without being further purified.
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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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