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General structure of carbodiimides: The core functional group is shown in blue with attached R groups

In organic chemistry, a carbodiimide is a functional group with the formula RN=C=NR. They are exclusively synthetic. A well known carbodiimide is dicyclohexylcarbodiimide, which is used in peptide synthesis.[1] Dialkylcarbodiimides are stable. Diaryl derivatives tend to convert to dimers and polymers upon standing at room temperature.[2]

Structure and bonding

From the perspective of bonding, carbodiimides are isoelectronic with carbon dioxide. Three principal resonance structures describe carbodiimides:


Relevant to the significance of the polar resonance structures, no carbodiimide has been separated into its optical isomers.[3]

The N=C=N core is nearly linear and the C-N=C angle is approximately 120″. The C=N distances are short, near 1.20 Å, characteristic of double bonds. The molecule are chiral, possessing C2-symmetry.[4]

The parent compound, methanediimine (HN=C=NH), is a tautomer of cyanamide.


From thioureas and ureas

A classic route to carbodiimides involves dehydrosulfurization of thioureas. A typical reagent is mercuric oxide:[5]

(R(H)N)2CS + HgO → (RN)2C + HgS + H2O

This reaction can often be conducted as stated, even though carbodiimides react with water. In some cases, a dehydrating agent is added to the reaction mixture.

The dehydration of N,N'-dialkylureas gives carbodiimides:

(R(H)N)2CO → (RN)2C + H2O

Phosphorus pentoxide[3] and p-Toluenesulfonyl chloride have been used as a dehydrating agents.[6][7]

From isocyanates

Isocyanates convert to carbodiimides with loss of carbon dioxide:[8][2]

2 RC=N=O → (RN)2C + CO2

The reaction is catalyzed by phosphine oxides. This reaction is reversible.[5]


Carbodiimides exhibit the reactivity characteristic of CO2, but is less electrophilic. Nucleophiles add to carbon. In this way, specialty guanidines can be prepared.[1] As weak bases, carbodiimides bind to Lewis acids to give adducts.[5]

Moffatt oxidation

Carbodiimides are reagents for the Moffatt oxidation, a protocol for conversion of an alcohol to a carbonyl (ketone or aldehyde). Dimethyl sulfoxide is the other component on this protocol:[9]

(CH3)2SO + (CyN)2C + R2CHOH → (CH3)2S + (CyNH)2CO + R2C=O

Typically the sulfoxide and diimide are used in excess.[10] The reaction cogenerates dimethyl sulfide and a urea.

Coupling agents

In synthetic, compounds containing the carbodiimide functionality are used as dehydration agents. Specifically they are often used to convert carboxylic acids to amides or esters. Additives, such as N-hydroxybenzotriazole or N-hydroxysuccinimide, are often added to increase yields and decrease side reactions.

Amide coupling utilizing a carbodiimide

Polycarbodiimides can also be used as crosslinkers for aqueous resins, such a polyurethane dispersions or acrylic dispersion. Here the polycarbodiimide reacts with carboxylic acids, which functional groups are often present in such aqueous resins, to form N-acyl urea. The result is that there have formed covalent bonds between the polymer chains, which have thus become crosslinked. [11][12]

Amide formation mechanism

The formation of an amide using a carbodiimide is straightforward, but with several side reactions complicating the subject. The acid 1 will react with the carbodiimide to produce the key intermediate: the O-acylisourea 2, which can be viewed as a carboxylic ester with an activated leaving group. The O-acylisourea will react with amines to give the desired amide 3 and urea 4.

The side reaction of the O-acylisourea 2 produce both desired and undesired products. The O-acylisourea 2 can react with an additional carboxylic acid 1 to give an acid anhydride 5, which can react further to give the desired amide 3. The main undesired reaction pathway involves the rearrangement of the O-acylisourea 2 to the stable N-acylurea 6. The use of solvents with low-dielectric constants such as dichloromethane or chloroform can minimize this side reaction.[13]

The reaction mechanism of amide formation using a carbodiimide.



DCC (acronym for N,N'-dicyclohexylcarbodiimide) was one of the first carbodiimides developed as a reagent. It is widely used for amide and ester formation, especially for solid-phase peptide synthesis. DCC has achieved popularity mainly because of its high yielding amide coupling reactions and the fact that it is quite inexpensive.

However, DCC does have some serious drawbacks, and its use is often avoided for several reasons:

  1. The byproduct N,N'-dicyclohexylureais mostly removed by filtration, but trace impurities can be difficult to remove. It is incompatible with traditional solid-phase peptide synthesis.
  2. DCC is a potent allergen, repeated contact with skin increases the probability of sensitization to the compound. Clinical reports of individuals who cannot enter rooms where peptide coupling agents are used have been reported.

For alternative to DCC in coupling see (Coupling Reagents BOP, DCC) at :


In contrast to DCC, DIC (acronym for N,N'-diisopropylcarbodiimide) is a liquid and its hydrolysis product N,N'-diisopropylurea, is soluble in organic solvents.


EDC is a water-soluble carbodiimide reagent used for a wide range of purposes. Apart from uses related to DCC and DIC, it is also used for various biochemical experiments as a crosslinker or chemical probe.


1-cyclohexyl-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate is a carbodiimide developed for the chemical probing of RNA structure in biochemistry.


  1. ^ a b Andrew Williams, Ibrahim T. Ibrahim (1981). "Carbodiimide Chemistry: recent Advances". Chem. Rev. 81: 589–636. doi:10.1021/cr00046a004.CS1 maint: Uses authors parameter (link)
  2. ^ a b T. W. Campbell, J. J. Monagle (1963). "Diphenylcarbodiimide". Org. Synth. 43: 31. doi:10.15227/orgsyn.043.0031.CS1 maint: Uses authors parameter (link)
  3. ^ a b Henri Ulrich (2008). Chemistry and Technology of Carbodiimides. Wiley-VCH. ISBN 978-0-470-06510-5.
  4. ^ A. T. Vincent, P. J. Wheatley (1972). "Crystal structure of bis-p-nitrophenylcarbodi-imide, O2N·C6H4·N:C:N·C6H4·NO2". Journal of the Chemical Society, Perkin Transactions 2: 1567–1571. doi:10.1039/P29720001567.CS1 maint: Uses authors parameter (link)
  5. ^ a b c Frederick Kurzer, K. Douraghi-Zadeh (1967). "Advances in the Chemistry of Carbodiimides". Chem. Rev. 67: ee107–152. doi:10.1021/cr60246a001.CS1 maint: Uses authors parameter (link)
  6. ^ John C. Sheehan, Philip A. Cruickshank (1968). "1-Ethyl-3-(3-Dimethylamino)propylcarbodiimide Hydrochloride and Methiodide". Org. Synth. 48: 83. doi:10.15227/orgsyn.048.0083.CS1 maint: Uses authors parameter (link)
  7. ^ Arnab K. Maity, Skye Fortier, Leonel Griego, Alejandro J. Metta-Magaña (2014). "Synthesis of a "Super Bulky" Guanidinate Possessing an Expandable Coordination Pocket". Inorg. Chem. 53: 8155–8164. doi:10.1021/ic501219q.CS1 maint: Uses authors parameter (link)
  8. ^ Monagle, J. J. (1962). "Carbodiimides. III. Conversion of Isocyanates to Carbodiimides. Catalyst Studies". J. Org. Chem. 27 (11): 3851–3855. doi:10.1021/jo01058a022.
  9. ^ Tidwell, T. T. (1990). "Oxidation of Alcohols by Activated Dimethyl Sulfoxide and Related Reactions: An Update". Synthesis: 857–870. doi:10.1055/s-1990-27036.
  10. ^ John G. Moffatt (1967). "Cholane-24-al". Org. Synth. 47: 25. doi:10.15227/orgsyn.047.0025.
  11. ^ Hesselmans, L.C.J.; Derksen, A.J.; van den Goorbergh, J.A.M. (2006). "Polycarbodiimide crosslinkers". Progress in Organic Coatings. 55 (2): 142–148. doi:10.1016/j.porgcoat.2005.08.011. ISSN 0300-9440.
  12. ^ Posthumus, W.; Derksen, A.J.; van den Goorbergh, J.A.M.; Hesselmans, L.C.J. (2007). "Crosslinking by polycarbodiimides". Progress in Organic Coatings. 58 (2–3): 231–236. doi:10.1016/j.porgcoat.2006.09.031. ISSN 0300-9440.
  13. ^ Hotan Mojarradi (2010). Coupling of substances containing a primary amine to hyaluronan via carbodiimide-mediated amidation (Thesis). Uppsala Universitet. ISSN 1650-8297.
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