Ester

Related Topics:
Esterel,_Jacques :: Ester :: Estero :: Esterhazy :: Esterified_Estrogens_and_Methyltestosterone :: Esterillos_Oeste

In chemistry, esters are organic compounds in which an organic group (symbolized by R' in this article) replaces a hydrogen atom (or more than one) in an oxygen acid. An oxygen acid is an acid whose molecule has an - group from which the hydrogen (H) can dissociate as an H⁺ ion.

The most common esters are the carboxylate esters, where the acid in question is a carboxylic acid. For example, if the acid is acetic acid, the ester is called an acetate. Esters may also be formed with inorganic acids; for example, dimethyl sulfate is an ester, and sometimes called "sulfuric acid, dimethyl ester".

Esters are named similarly to salts; although they don't really have cations and anions, the terminology follows the same pattern: a more electropositive part followed by a more electronegative part.

An ester can be thought of as a product of a condensation reaction of an acid (usually an organic acid) and an alcohol (or phenol compound), although there are other ways to form esters. Condensation is a type of chemical reaction in which two molecules with -OH groups are joined with eliminating a water molecule from their -OH groups. A condensation reaction to form an ester is called esterification. Esterification can be catalysed by the presence of H⁺ ions. Sulfuric acid is often used as a catalyst for this reaction. The name ester is derived from the German Essig-Äther, an old name for acetic acid ethyl ester (ethyl acetate).

Naming of esters

Esters can be produced by an equilibrium reaction between an alcohol and a carboxylic acid. The ester is named according to the alkyl group (the part from the alcohol) and then the alkanoate (the part from the carboxylic acid) which make it up.IUPAC naming of esters For example, the reaction between methanol and butyric acid yields the ester methyl butyrate C₃H₇-COO-CH₃ (as well as water). The simplest ester is H-COO-CH₃ (methyl formate, also called methyl methanoate).

For esters derived from the simplest carboxylic acids, the traditional names are recommended by IUPAC,IUPAC parent groups using traditional names viz, formate, acetate, propionate, butyrate, though out of these only acetate may carry further substituents. For esters from higher acids, the alkane name with an -oate ending is generally preferred, e.g., hexanoate. Common esters of aromatic acids include benzoates such as methyl benzoate, and phthalates, with substitution allowed in the name.

Physical properties

Esters participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding makes them more water-soluble than their parent hydrocarbons. However, the limitations on their hydrogen bonding also make them more hydrophobic than either their parent alcohols or parent acids. Their lack of hydrogen-bond-donating ability means that ester molecules cannot hydrogen-bond to each other, which makes esters generally more volatile than an carboxylic acid of similar molecular weight. This property makes them very useful in organic analytical chemistry: unknown organic acids with low volatility can often be esterified into a volatile ester, which can then be analysed using gas chromatography, gas liquid chromatography, or mass spectrometry. Many esters have distinctive odors, which has led to their widespread use as artificial flavorings and fragrances. For example:

methyl butyrate smells of pineapple or apple

methyl salicylate (oil of wintergreen) smells of the ointments called Germolene™ and Ralgex™ in the UK

methyl benzoate smells of fruity-ylang ylang

ethyl acetate smells of nail polish remover

ethyl formate smells of rum

ethyl butyrate smells of pineapple or strawberry

ethyl salicylate smells of oil of wintergreen

ethyl heptanoate smells of grape

ethyl valerate smells of apple

propyl isobutyrate smells of rum

isobutyl formate smells of raspberries

butyl butyrate smells of pineapple

pentyl acetate smells of banana

pentyl pentanoate smells of apple

pentyl butyrate smells of pear or apricot

isopentyl acetate smells of pear or banana (it is used as the flavouring in the manufacturing of old fashioned Pear Drops)

octyl acetate smells of fruity-orange

benzyl acetate smells slightly of jasmine

Ester synthesis

Esters can be prepared in the laboratory in several ways:

by esterification of carboxylic acid derivatives and alcohols
by transesterifications between other esters
by Dieckmann condensation or Claisen condensation of esters carrying acidic α-protons
by Favorskii rearrangement of α-haloketones in presence of base
by nucleophilic displacement of alkyl halides with carboxylic acid salts
by Baeyer-Villiger oxidation of ketones with peroxides
by Pinner reaction of nitriles with an alcohol

Ester reactions

Esters react in a number of ways:

Esters may undergo hydrolysis - the breakdown of an ester by water. This process can be catalyzed both by acids and bases. The base-catalyzed process is called saponification. The hydrolysis yields an alcohol and a carboxylic acid or its carboxylate salt.
Esters also react if heated with primary or secondary amines, producing amides.
Phenyl esters react to hydroxyarylketones in the Fries rearrangement.
Di-esters such as diethyl malonate react as nucleophile with alkyl halides in the malonic ester synthesis after deprotonation.
Specific esters are functionalized with an α-hydroxyl group in the Chan rearrangement
Esters are converted to isocyanates through intermediate hydroxamic acids in the Lossen rearrangement.

External links

Molecule of the month: Ethyl acetate and other esters
Making an Ester A simple guide to naming and making Esters, as well as the Chemistry behind it.

References

Functional groups | Esters | German loanwords