Ketene

Short description: Organic compound of the form >C=C=O

General formula for a ketene.

In organic chemistry, a ketene is an organic compound of the form RR'C=C=O, where R and R' are two arbitrary monovalent chemical groups (or two separate substitution sites in the same molecule).[1] The name may also refer to the specific compound ethenone H
2C=C=O, the simplest ketene.[2]

Although they are highly useful, most ketenes are unstable. When used as reagents in a chemical procedure, they are typically generated when needed, and consumed as soon as (or while) they are produced.[1]

## Contents

* 1 History
* 2 Properties
* 3 Synthesis
* 4 Reactions and applications
* 4.1 Formation of carboxylic acid esters
* 4.2 Formation of carboxylic anhydrides
* 4.3 Formation of amides
* 4.4 Hydrolysis
* 4.5 Formation of enol esters
* 4.6 Dimerisation
* 4.7 [2+2]-cycloaddition
* 4.8 Applications
* 5 See also
* 6 References
* 7 External links

## History

Ketenes were first studied as a class by Hermann Staudinger before 1905.[3]

Ketenes were systematically investigated by Hermann Staudinger in 1905 in the form of diphenylketene (conversion of [math]\displaystyle{ \alpha }[/math]-chlorodiphenyl acetyl chloride with zinc). Staudinger was inspired by the first examples of reactive organic intermediates and stable radicals discovered by Moses Gomberg in 1900 (compounds with triphenylmethyl group).[4]

## Properties

Ketenes are highly electrophilic at the carbon atom bonded with the heteroatom, due to its sp character. Ketene can be formed with different heteroatom bonded to the sp carbon atom, such as O, S or Se, respectively named ketene, thioketene and selenoketene.

Ethenone, the simplest ketene, has different experimental lengths for each of the double bonds; the C=O bond is 1,160Å and the C=C bond is 1,314Å. The angle between the two H atoms is 121.5°, similar to the theoretically ideal angle formed in alkenes between sp2 carbon atom and H substituents.[5]

Ketenes are unstable and cannot be stored. In the absence of nucleophiles with which to react, ethenone dimerises to give β-lactone, a cyclic ester. If the ketene is disubstituted, the dimerisation product is a substituted cyclobutadione. For monosubstituted ketenes, the dimerisation could afford either the ester or the diketone product.

## Synthesis

Ketene is produced on a commercial scale by thermal dehydration of acetic acid. Substituted ketenes can be prepared from acyl chlorides by an elimination reaction in which HCl is lost:

In this reaction, a base, usually triethylamine, removes the acidic proton alpha to the carbonyl group, inducing the formation of the carbon-carbon double bond and the loss of a chloride ion:

Ketenes can also be formed from α-diazoketones by the Wolff rearrangement.

Another way to generate ketenes is through flash vacuum thermolysis (FVT) with 2-pyridylamines. Plüg and Wentrup developed a method in 1997 that improved on FVT reactions to produce ketenes with a stable FVT that is moisture insensitive, using mild conditions (480 °C). The N-pyridylamines are prepared via a condensation with R-malonates with N-amino(pyridene) and DCC as the solvent.[6]

A more robust method for preparing ketenes is the carbonylation of metal-carbenes, and in situ reaction of the thus produced highly reactive ketenes with suitable reagents such as imines, amines, or alcohols.[7] This method is an efficient one‐pot tandem protocol of the carbonylation of α‐diazocarbonyl compounds and a variety of N‐tosylhydrazones catalysed by Co(II)–porphyrin metalloradicals leading to the formation of ketenes, which subsequently react with a variety of nucleophiles and imines to form esters, amides and β‐lactams. This system has a broad substrate scope and can be applied to various combinations of carbene precursors, nucleophiles and imines.[8]

## Reactions and applications

Due to their cumulated double bonds, ketenes are very reactive.[9]

### Formation of carboxylic acid esters

By reaction with alcohols, carboxylic acid esters are formed:

### Formation of carboxylic anhydrides

Ketenes react with a carboxylic acids to form carboxylic acid anhydrides:

### Formation of amides

Ketenes react with ammonia and amines to give the corresponding [amide]]s:

### Hydrolysis

By reaction with water, carboxylic acids are formed from ketenes

### Formation of enol esters

Enol esters are formed from ketenes with enolisable carbonyl compounds. The following example shows the reaction of ethenone with acetone to form a propen-2-yl acetate:

### Dimerisation

At room temperature, ketene quickly dimerizes to diketene, but the ketene can be recovered by heating:

### [2+2]-cycloaddition

Ketenes can react with alkenes, carbonyl compounds, carbodiimides and imines in a [2+2] cycloaddition. The example shows the synthesis of a β-lactam by the reaction of a ketene with an imine (see Staudinger synthesis):[10][11]

### Applications

Ketenes are generally very reactive, and participate in various cycloadditions. One important process is the dimerization to give propiolactones. A specific example is the dimerization of the ketene of stearic acid to afford alkyl ketene dimers, which are widely used in the paper industry.[1] AKD's react with the hydroxyl groups on the cellulose via esterification reaction.

They will also undergo [2+2] cycloaddition reactions with electron-rich alkynes to form cyclobutenones, or carbonyl groups to form beta-lactones. With imines, beta-lactams are formed. This is the Staudinger synthesis, a facile route to this important class of compounds. With acetone, ketene reacts to give isopropenyl acetate.[1]

A variety of hydroxylic compounds can add as nucleophiles, forming either enol or ester products. As examples, a water molecule easily adds to ketene to give 1,1-dihydroxyethene and acetic anhydride is produced by the reaction of acetic acid with ketene. Reactions between diols (HO–R–OH) and bis-ketenes (O=C=CH–R'–CH=C=O) yield polyesters with a repeat unit of (–O–R–O–CO–R'–CO).

Ethyl acetoacetate, an important starting material in organic synthesis, can be prepared using a diketene in reaction with ethanol. They directly form ethyl acetoacetate, and the yield is high when carried out under controlled circumstances; this method is therefore used industrially.

## See also

* Ynol
* Thioketene

## References

1. ↑ 1.0 1.1 1.2 1.3 Miller, Raimund; Abaecherli, Claudio; Said, Adel; Jackson, Barry (2001). "Ketenes". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a15_063. ISBN 978-3527306732.
2. ↑ Saul Patai, ed (1980). Ketenes, Allenes and Related Compounds: Part 1, Volume 1. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. doi:10.1002/9780470771600. ISBN 9780470771600. Saul Patai, ed (1980). Ketenes, Allenes and Related Compounds: Part 2, Volume 2. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. doi:10.1002/9780470771617. ISBN 9780471276708.
3. ↑ Staudinger, Hermann (1905). "Ketene, eine neue Körperklasse". Berichte der Deutschen Chemischen Gesellschaft 38 (2): 1735–1739. doi:10.1002/cber.19050380283. http://babel.hathitrust.org/cgi/pt?id=uc1.b3481909;view=1up;seq=483.
4. ↑ Thomas T. Tidwell, The first century of Ketenes (1905-2005): the birth of a family of reactive intermediates, Angewandte Chemie, Int. Edition, Band 44, 2005, S. 5778–5785
5. ↑ Ma, Ngai Ling; Wong, MingWah (2000). "A Theoretical Study of the Properties and Reactivities of Ketene, Thioketene, and Selenoketene". European Journal of Organic Chemistry 2000 (8): 1411_1421. doi:10.1002/(SICI)1099-0690(200004)2000:8<1411::AID-EJOC1411>3.0.CO;2-N. https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/(SICI)1099-0690(200004)2000:8<1411::AID-EJOC1411>3.0.CO;2-N.
6. ↑ Carsten Plüg ,Hussein Kanaani and Curt Wentrup (12 February 2015). "Ketenes from N-(2-Pyridyl)amides". Australian Journal of Chemistry 68 (4): 687. doi:10.1071/CH14714.
7. ↑ "Carbene radicals in cobalt(II)-porphyrin-catalysed carbene carbonylation reactions; a catalytic approach to ketenes". Chemistry: A European Journal 19 (39): 12953–8. September 2013. doi:10.1002/chem.201301731. PMID 24038393.
8. ↑ "[Co(MeTAA) Metalloradical Catalytic Route to Ketenes via Carbonylation of Carbene Radicals"] (in en). European Journal of Inorganic Chemistry 2018 (20–21): 2251–2258. 2018. doi:10.1002/ejic.201800101. ISSN 1099-0682. https://pure.uva.nl/ws/files/34388611/Chirila_et_al_2018_European_Journal_of_Inorganic_Chemistry.pdf.
9. ↑ Siegfried Hauptmann (1985) (in de), Organische Chemie: mit 65 Tabellen, Leipzig: Deutscher Verlag für Grundstoffindustrie, pp. 410–412, ISBN 3871449024
10. ↑ Jie Jack Li (2006) (in de), Name reactions. A collection of detailed reaction mechanisms (3 ed.), Berlin: Springer-Verlag, pp. 561-562, doi:10.1007/3-540-30031-7, ISBN 9783540300304
11. ↑ Hermann Staudinger (1907), "Zur Kenntnis der Ketene. Diphenylketen" (in de), Justus Liebigs Annalen der Chemie (John Wiley & Sons, Inc.) 356 (1–2): pp. 51–123, doi:10.1002/jlac.19073560106, https://zenodo.org/record/1427571

## External links

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Molecules detected in outer space

Molecules|

| Diatomic|

* Aluminium monochloride
* Aluminium monofluoride
* Aluminium monoxide
* Argonium
* Carbon monophosphide
* Carbon monosulfide
* Carbon monoxide
* Carborundum
* Cyanogen radical
* Diatomic carbon
* Fluoromethylidynium
* Helium hydride ion
* Hydrogen chloride
* Hydrogen fluoride
* Hydrogen (molecular)
* Hydroxyl radical
* Iron(II) oxide
* Magnesium monohydride cation
* Methylidyne radical
* Nitric oxide
* Nitrogen (molecular)
* Nitrogen monohydride
* Nitrogen sulfide
* Oxygen (molecular)
* Phosphorus monoxide
* Phosphorus mononitride
* Potassium chloride
* Silicon carbide
* Silicon mononitride
* Silicon monoxide
* Silicon monosulfide
* Sodium chloride
* Sodium iodide
* Sulfur monohydride
* Sulfur monoxide
* Titanium oxide

|
|

Triatomic|

* Aluminium hydroxide
* Aluminium isocyanide
* Amino radical
* Carbon dioxide
* Carbonyl sulfide
* CCP radical
* Chloronium
* Diazenylium
* Dicarbon monoxide
* Disilicon carbide
* Ethynyl radical
* Formyl radical
* Hydrogen cyanide (HCN)
* Hydrogen isocyanide (HNC)
* Hydrogen sulfide
* Hydroperoxyl
* Iron cyanide
* Isoformyl
* Magnesium cyanide
* Magnesium isocyanide
* Methylene radical
* N2H+
* Nitrous oxide
* Nitroxyl
* Ozone
* Phosphaethyne
* Potassium cyanide
* Protonated molecular hydrogen
* Sodium cyanide
* Sodium hydroxide
* Silicon carbonitride
* c-Silicon dicarbide
* SiNC
* Sulfur dioxide
* Thioformyl
* Thioxoethenylidene
* Titanium dioxide
* Tricarbon
* Water

Four
atoms|

* Acetylene
* Ammonia
* Cyanic acid
* Cyanoethynyl
* Cyclopropynylidyne
* Formaldehyde
* Fulminic acid
* HCCN
* Hydrogen peroxide
* Hydromagnesium isocyanide
* Isocyanic acid
* Isothiocyanic acid
* Ketenyl
* Methylene amidogen
* Methyl radical
* Propynylidyne
* Protonated carbon dioxide
* Protonated hydrogen cyanide
* Silicon tricarbide
* Thioformaldehyde
* Tricarbon monoxide
* Tricarbon sulfide
* Thiocyanic acid

Five
atoms|

* Ammonium ion
* Butadiynyl
* Carbodiimide
* Cyanamide
* Cyanoacetylene
* Cyanoformaldehyde
* Cyanomethyl
* Cyclopropenylidene
* Formic acid
* Isocyanoacetylene
* Ketene
* Methane
* Methoxy radical
* Methylenimine
* Propadienylidene
* Protonated formaldehyde
* Protonated formaldehyde
* Silane
* Silicon-carbide cluster

Six
atoms|

* Acetonitrile
* Cyanobutadiynyl radical
* E-Cyanomethanimine
* Cyclopropenone
* Diacetylene
* Ethylene
* Formamide
* HC4N
* Ketenimine
* Methanethiol
* Methanol
* Methyl isocyanide
* Pentynylidyne
* Propynal
* Protonated cyanoacetylene

Seven
atoms|

* Acetaldehyde
* Acrylonitrile
* Vinyl cyanide
* Cyanodiacetylene
* Ethylene oxide
* Glycolonitrile
* Hexatriynyl radical
* Methylacetylene
* Methylamine
* Methyl isocyanate
* Vinyl alcohol

Eight
atoms|

* Acetic acid
* Aminoacetonitrile
* Cyanoallene
* Ethanimine
* Glycolaldehyde
* Heptatrienyl radical
* Hexapentaenylidene
* Methylcyanoacetylene
* Methyl formate
* Propenal

Nine
atoms|

* Acetamide
* Cyanohexatriyne
* Cyanotriacetylene
* Dimethyl ether
* Ethanol
* Methyldiacetylene
* Octatetraynyl radical
* Propene
* Propionitrile

Ten
atoms
or more|

* Acetone
* Benzene
* Benzonitrile
* Buckminsterfullerene (C60, C60+, fullerene, buckyball)
* C70 fullerene
* Cyanodecapentayne
* Cyanopentaacetylene
* Cyanotetra-acetylene
* Ethylene glycol
* Ethyl formate
* Methyl acetate
* Methyl-cyano-diacetylene
* Methyltriacetylene
* Propanal
* n-Propyl cyanide
* Pyrimidine

Deuterated
molecules|

* Ammonia
* Ammonium ion
* Formaldehyde
* Formyl radical
* Heavy water
* Hydrogen cyanide
* Hydrogen deuteride
* Hydrogen isocyanide
* Methylacetylene
* N2D+
* Trihydrogen cation

Unconfirmed|

* Anthracene
* Dihydroxyacetone
* Ethyl methyl ether
* Glycine
* Graphene
* H2NCO+
* Linear C5
* Naphthalene cation
* Phosphine
* Pyrene
* Silylidine

Related|

* Abiogenesis
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* Atomic and molecular astrophysics
* Chemical formula
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* Diffuse interstellar band
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* Extraterrestrial liquid water
* Forbidden mechanism
* Homochirality
* Intergalactic dust
* Interplanetary medium
* Interstellar medium
* Photodissociation region
* Iron–sulfur world theory
* Kerogen
* Molecules in stars
* Nexus for Exoplanet System Science
* Organic compound
* Outer space
* PAH world hypothesis
* Panspermia
* Polycyclic aromatic hydrocarbon (PAH)
* RNA world hypothesis
* Spectroscopy
* Tholin

* Category:Astrochemistry
*   *   *

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