Examples of 'saturated aqueous ammonium chloride' in a sentence
Meaning of "saturated aqueous ammonium chloride"
A solution composed of ammonium chloride dissolved in water to its maximum limit, resulting in a saturated solution
How to use "saturated aqueous ammonium chloride" in a sentence
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saturated aqueous ammonium chloride
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.
Of saturated aqueous ammonium chloride.
This solution was extracted with saturated aqueous ammonium chloride.
Saturated aqueous ammonium chloride is added and extracted with EtOAc.
The reaction quenched by adding saturated aqueous ammonium chloride.
Saturated aqueous ammonium chloride was added and extracted with EtOAc.
It is then poured into saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride and ethyl acetate were added to the solution.
The preferred acid is saturated aqueous ammonium chloride solution.
Saturated aqueous ammonium chloride and EtOAc were added and the mixture was filtered.
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.
See also
saturated aqueous
saturated aqueous ammonium
saturated aqueous sodium
saturated aqueous sodium bicarbonate
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.
A saturated aqueous ammonium chloride solution and ethyl acetate were added to the mixture.
The combined extracts are washed with saturated aqueous ammonium chloride and evaporated.
Water and saturated aqueous ammonium chloride were added thereto for partitioning the mixture.
The combined extracts were washed with saturated aqueous ammonium chloride and evaporated.
ML of a saturated aqueous ammonium chloride solution were added.
The resulting crystals were dissolved in ethyl acetate and a saturated aqueous ammonium chloride solution.
After hydrolysis with saturated aqueous ammonium chloride tetrahydrofuran was evaporated under reduced pressure.
Cool the reaction to room temperature and pour into saturated aqueous ammonium chloride.
Quench the reaction with saturated aqueous ammonium chloride and extract into ethyl acetate.
After stirring overnight at room temperature the mixture is treated with saturated aqueous ammonium chloride.
Reaction was quenched with saturated aqueous ammonium chloride and phases were separated.
Dissolve the residue in EtOAc and wash the organic solution with saturated aqueous ammonium chloride.
The mixture is quenched with saturated aqueous ammonium chloride and warmed to room temperature.
Dilute the resulting suspension with DCM and quench with saturated aqueous ammonium chloride.
Pour the solution into saturated aqueous ammonium chloride and extract into ethyl ether.
When the reaction is brought to rt, it is quenched 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.
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.
Wash the combined organic solutions with saturated aqueous ammonium chloride and saturated NaCl.
Excess saturated aqueous ammonium chloride was added to the mixture followed by 200 ml EtOAc.
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.
Add saturated aqueous ammonium chloride and extract with ethyl acetate ( 2X ).
The excess sodium borohydride was decomposed with saturated aqueous ammonium chloride and extracted with EtOAc.
Saturated aqueous ammonium chloride solution ( 2 mL ) was added.
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