Structural Biochemistry/Organic Chemistry/Methods of Separation and Isolation
Extraction is a technique used for separating a compound from a mixture. An example is separating a water-insoluble organic compound from an aqueous mixture by extracting it into a water-insoluble organic solvent. These extractions are often part of the workup procedure for isolating and purifying the product of an organic reaction. Because trace amounts of water are often present at the end of an extraction process, a drying reagent is needed to ensure a dry product. The process of liquid-liquid extraction involves the distribution of a compound between two solvents that are insoluble in each other. By taking advantage of the differing solubilities of a solute in a pair of solvents, compounds can be selectively transported from one liquid phase to the other.
This occurrence is quantified by the partition coefficient (K):
The larger the value of K, the solute will be found in greater amounts in the organic solvent. In an extraction procedure, an aqueous phase, usually water, and a immiscible organic solvent known as the organic phase are generally shaken in a container. The solutes are then allowed to distribute themselves between the two layers according to their solubility, the denser layer is always on the bottom of the container. After they have distributed themselves, each layer can be removed and analyzed separately by drying the extractions. The factors that need to be considered in selecting a drying agent are its capacity for removing water, its efficiency, the speed with which it works, and its chemical inertness. Once the extraction has been dried, the solvent must be removed to recover the desired organic product. This can be achieved by heating the container of the mixture and allowing for the solvent to evaporate, leaving a solid or liquid residue or allowing the mixture in to evaporate in a fume hood, depending on the volatility of the solvent.
Liquid-Liquid Extraction FlowChart
You want to isolate a mixture of compounds, and you do this by taking advantage of the bascicity and acidity of certain compounds. It is also important to note those structures that are rather neutral. Some key concepts are, bases will react with acid and vice versa. Also, the aqueous layer will contain a charged molecule, or ion, most of the time.
Step 1: Upon dissolving the mixture in a good solvent such as methylene chloride, a strong acid is added to the mixture.
The strong acid is added so that it will react with any basic compounds in the mixture, which wil lead it into the aqueous layer. Thus, one of the compounds has been separated. Adding base will deprotonate the proton from the nitrogen and give you the isolated product in the organic layer.
Step 2: To the remaining 3 compounds, a weak base is added, such as sodium carbonate.
The weak base will deprotonate the most acidic of the hydrogens, which is in this case, the carboxylic acid. The carboxylic acid containing structuer will be separated into the aqueous layer. Keep in mind, that the base is not limited to only deprotonating one structure, but this all just depends on the acidity of the compounds.
Step 3: To the final 2 compounds, a stronger base such as potassium hydroxide which will deprotonate the phenol.
Generally phenols are not very acidic, that is why a strong base must be used. The cyano containing compound is left in the organic layer.
Reaction Complete. All 4 compounds have been isolated into either aqueous or organic, and as mentioned eariler, it is very easy to bring an aqueous compound back into the organic, that is by adding the complementary acid or base.
Column chromatography is a preparative method for separating and isolating compounds from mixtures which can later be analyzed using thin-layer chromatography (TLC), gas chromatography, or IR. The method is used for obtaining compounds from natural sources or for purifying products from reaction mixtures. This method can be considered an upside-down version of TLC. Instead of having a thin layer of adsorbent attached to a solid support, a column is filled with a larger amount of adsorbent, often silica gel, and the mixture is loaded on top of it. While TLC depends on capillary action, column chromatography depends on a solvent or eluent moving down the column using the force of gravity. As this eluent moves down the column, it carries the soluble compounds with it and compounds having strong interactions with the adsorbent move more slowly than compounds having weaker interactions with the adsorbent. By taking advantage of the material used for the stationary and mobile phase, the compounds will separate in distinctive bands and each band will come out of the column individually. This will allow for the collection of each separate band in different vials which can then be analyzed with TLC and then dried to later be analyzed based on their melting points.
Polarity plays a large role in the process, where the using a non-polar solvent allows for a non-polar substance to be collected first before the more polar components. As the polarity of the solvents increase, more polar compounds travel further faster. This is why it is important for the solvents used to slowly change in polarity throughout the column chromatography procedure for better separation.