Examples of 'saturated aqueous ammonium' in a sentence
Meaning of "saturated aqueous ammonium"
saturated aqueous ammonium: a chemical solution where the maximum amount of ammonium has been dissolved in water
How to use "saturated aqueous ammonium" in a sentence
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saturated aqueous ammonium
Added thereto was a saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride was added.
Reaction was quenched by addition of saturated aqueous ammonium chloride.
Saturated aqueous ammonium sulfate is added.
This solution was extracted with saturated aqueous ammonium chloride.
Of saturated aqueous ammonium chloride.
The reaction quenched by adding saturated aqueous ammonium chloride.
Saturated aqueous ammonium chloride is added and extracted with EtOAc.
It is then poured into saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride was added and extracted with EtOAc.
The preferred acid is saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride and ethyl acetate were added to the solution.
To the cooled reaction mixture is added saturated aqueous ammonium chloride.
Add saturated aqueous ammonium chloride and separated the layers.
Extract the organic layer with saturated aqueous ammonium chloride solution.
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Add saturated aqueous ammonium chloride and dilute with ethyl acetate.
The reaction medium is poured onto a saturated aqueous ammonium chloride solution.
Thereafter a saturated aqueous ammonium chloride solution was dropwise added under cooling.
The reaction medium is neutralized by the addition of a saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride and EtOAc were added and the mixture was filtered.
Reaction was quenched with saturated aqueous ammonium chloride and phases were separated.
Saturated aqueous ammonium sulphate was then added and the solution extracted with ether.
The combined extracts are washed with saturated aqueous ammonium chloride and evaporated.
A saturated aqueous ammonium chloride solution and ethyl acetate were added to the mixture.
The combined extracts were washed with saturated aqueous ammonium chloride and evaporated.
Water and saturated aqueous ammonium chloride were added thereto for partitioning the mixture.
The residue was taken up between ethyl acetate and saturated aqueous ammonium hydrochloride.
After hydrolysis with saturated aqueous ammonium chloride tetrahydrofuran was evaporated under reduced pressure.
The resulting crystals were dissolved in ethyl acetate and a saturated aqueous ammonium chloride solution.
Quench the reaction with saturated aqueous ammonium chloride and extract into ethyl acetate.
Cool the reaction to room temperature and pour into saturated aqueous ammonium chloride.
Pour the solution into saturated aqueous ammonium chloride and extract into ethyl ether.
After stirring overnight at room temperature the mixture is treated with saturated aqueous ammonium chloride.
The mixture is quenched with saturated aqueous ammonium chloride and warmed to room temperature.
The reaction was concentrated in vacuo and the reaction neutralised with saturated aqueous ammonium hydroxide.
The aqueous phase is treated with a saturated aqueous ammonium chloride solution and extracted with dichloromethane.
Dissolve the residue in EtOAc and wash the organic solution with saturated aqueous ammonium chloride.
Wash the filtrate with saturated aqueous ammonium chloride solution and saturated aqueous sodium bicarbonate solution.
Deprotection is accomplished with mild acid such as saturated aqueous ammonium chloride or citric acid.
ML of a saturated aqueous ammonium chloride solution were added.
Wash the combined organic solutions with saturated aqueous ammonium chloride and saturated NaCl.
Saturated aqueous ammonium chloride was then added, followed by ethyl acetate.
The reaction mixture was treated with saturated aqueous ammonium chloride followed by ethyl acetate.
Saturated aqueous ammonium chloride was added, and the aqueous phase was separated.
The resulting solution was washed with saturated aqueous ammonium chloride and the phases separated.
A saturated aqueous ammonium chloride solution was added thereto, and insoluble material was filtered off.
The combined organic phases were washed once more with saturated aqueous ammonium chloride solution.
Then 30 mL of a saturated aqueous ammonium chloride solution were added.
Dissolve the residue in methylene chloride and wash with saturated aqueous ammonium chloride and brine.
Saturated aqueous ammonium bicarbonate was added until the pH was > 7.
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