Acyl chloride
In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids (R−C(=O)OH). A specific example of an acyl chloride is acetyl chloride, CH3COCl. Acyl chlorides are the most important subset of acyl halides.
Nomenclature
Where the acyl chloride moiety takes priority, acyl chlorides are named by taking the name of the parent carboxylic acid, and substituting -yl chloride for -ic acid. Thus:
- acetic acid (CH3COOH) → acetyl chloride (CH3COCl)
- benzoic acid (C6H5COOH) → benzoyl chloride (C6H5COCl)
- butyric acid (C3H7COOH) → butyryl chloride (C3H7COCl)
(Idiosyncratically, for some trivial names, -oyl chloride substitutes -ic acid. For example, pivalic acid becomes pivaloyl chloride and acrylic acid becomes acryloyl chloride. The names pivalyl chloride and acrylyl chloride are less commonly used, although they are arguably more logical.)
When other functional groups take priority, acyl chlorides are considered prefixes — chlorocarbonyl-:[1]
- acetic acid (CH3COOH) → (chlorocarbonyl)acetic acid (ClOCCH2COOH)
Properties
Lacking the ability to form
The simplest stable acyl chloride is acetyl chloride; formyl chloride is not stable at room temperature, although it can be prepared at –60 °C or below.[2][3]
Acyl chlorides hydrolyze (react with water) to form the corresponding carboxylic acid and hydrochloric acid:
Synthesis
Industrial routes
The industrial route to acetyl chloride involves the reaction of acetic anhydride with hydrogen chloride:[5]
Propionyl chloride is produced by chlorination of propionic acid with phosgene:[6]
Benzoyl chloride is produced by the partial hydrolysis of benzotrichloride:[7]
Similarly, benzotrichlorides react with carboxylic acids to the acid chloride. This conversion is practiced for the reaction of 1,4-bis(trichloromethyl)benzene to give terephthaloyl chloride:
Laboratory methods: thionyl chloride
In the laboratory, acyl chlorides are generally prepared by treating carboxylic acids with thionyl chloride (SOCl2).[8] The reaction is catalyzed by dimethylformamide and other additives.[9][10]
Thionyl chloride[11] is a well-suited reagent as the by-products (HCl, SO2) are gases and residual thionyl chloride can be easily removed as a result of its low boiling point (76 °C).
Laboratory methods: phosphorus chlorides
Phosphorus trichloride (PCl3) is popular,[12] although excess reagent is required.[9] Phosphorus pentachloride (PCl5) is also effective,[13][14] but only one chloride is transferred:
Laboratory methods: oxalyl chloride
Another method involves the use of oxalyl chloride:
The reaction is catalysed by dimethylformamide (DMF), which reacts with oxalyl chloride to give the Vilsmeier reagent, an iminium intermediate that which reacts with the carboxylic acid to form a mixed imino-anhydride. This structure undergoes an acyl substitution with the liberated chloride, forming the acid anhydride and releasing regenerated molecule of DMF.[10] Relative to thionyl chloride, oxalyl chloride is more expensive but also a milder reagent and therefore more selective.
Other laboratory methods
Acid chlorides can be used as a chloride source.[15] Thus acetyl chloride can be distilled from a mixture of benzoyl chloride and acetic acid:[9]
Other methods that do not form HCl include the Appel reaction:[16]
Another is the use of cyanuric chloride:[17]
Reactions
Acyl chloride are reactive, versatile reagents.[18] Acyl chlorides have a greater reactivity than other carboxylic acid derivatives like acid anhydrides, esters or amides:
Nucleophilic reactions
Acid chlorides are useful for the preparation of amides, esters, anhydrides. These reactions generate chloride, which can be undesirable. Acyl chlorides hydrolyze, yielding the carboxylic acid:
This hydrolysis is usually a nuisance rather than intentional. Acyl chlorides are used to prepare acid anhydrides, amides and esters, by reacting acid chlorides with: a salt of a carboxylic acid, an amine, or an alcohol, respectively.
Mechanism
The alcoholysis of acyl halides (the alkoxy-dehalogenation) is believed to proceed via an SN2 mechanism (Scheme 10).[19] However, the mechanism can also be tetrahedral or SN1 in highly polar solvents[20] (while the SN2 reaction involves a concerted reaction, the tetrahedral addition-elimination pathway involves a discernible intermediate).[21]
Bases, such as pyridine or N,N-dimethylformamide, catalyze acylations.[14][10] These reagents activate the acyl chloride via a nucleophilic catalysis mechanism. The amine attacks the carbonyl bond and presumably[22] first forms a transient tetrahedral intermediate, then forms a quaternary acylammonium salt by the displacement of the leaving group. This quaternary acylammonium salt is more susceptible to attack by alcohols or other nucleophiles.
The use of two phases (aqueous for amine, organic for acyl chloride) is called the
Conversion to ketones
Carbon nucleophiles such as
Reduction
Acyl chlorides are reduced by
Acylation of arenes
With
Because of the harsh conditions and the reactivity of the intermediates, this otherwise quite useful reaction tends to be messy, as well as environmentally unfriendly.
Oxidative addition
Acyl chlorides react with low-valent metal centers to give transition metal acyl complexes. Illustrative is the oxidative addition of acetyl chloride to Vaska's complex, converting square planar Ir(I) to octahedral Ir(III):[26]
Hazards
Low molecular weight acyl chlorides are often
References
- ^ Nomenclature of Organic Chemistry, R-5.7.6 Acid halides
- ISBN 9780471936237
- ISBN 978-0-7487-6162-3.
- PMID 21577915.
- ^ US patent 5672749, Phillip R. DeVrou, W. Bryan Waites, Robert E. Young, "Process for preparing acetyl chloride"
- ISBN 978-3527306732.
- ISBN 978-3527306732.
- .
- ^ ISBN 9780470771273.
- ^ ISBN 0-19-850346-6.
- ^ J. S. Pizey, Synthetic Reagents, Vol. 1, Halsted Press, New York, 1974.
- ^ .
- .
- ^ ISBN 0-13-643669-2.
- .
- ^ "Triphenylphosphine-carbon tetrachloride Taschner, Michael J. e-EROS: Encyclopedia of Reagents for Organic Synthesis, 2001
- .
- ISSN 0009-2665.
- PMID 11667754.
- ^ C. H. Bamford and C. F. H. Tipper, Comprehensive Chemical Kinetics: Ester Formation and Hydrolysis and Related Reactions, Elsevier, Amsterdam, 1972.
- PMID 15471486.
- PMID 11672060.
- ISSN 0021-9584.
- ISBN 978-0471264187.
- ^ William Reusch. "Carboxylic Acid Derivatives". VirtualText of Organic Chemistry. Michigan State University. Archived from the original on 2016-05-16. Retrieved 2009-02-19.
- ISBN 978-1-938787-15-7.