| Identification | Back Directory | [Name]
diphenylcarbodiimide | [CAS]
622-16-2 | [Synonyms]
carbodiphenylimide
diphenylcarbodiimide
Bis(phenylimino)methane
N,N'-Diphenylcarbodiimide
N,N'-Diphenylmethanediimine
N,N'-methanediylidenedianiline
phenyl(phenyliminomethylene)amine
Benzenamine, N,N-methanetetraylbis-
BenzenaMine,N,N'-Methanetetraylbis- or diphenyl carbodiiMide | [EINECS(EC#)]
210-721-4 | [Molecular Formula]
C13H10N2 | [MOL File]
622-16-2.mol | [Molecular Weight]
194.23 |
| Hazard Information | Back Directory | [Preparation]
Triphenylphosphine (2.62 g, 0.01 mol) in THF (10 mL) was added dropwise to N,N'-diphenylthiourea (2.28 g, 0.01 mol) and diethyl azodicarboxylate (1.74 g, 0.01 mol) in THF (20 mL) at room temperature. After standing overnight, the solvent was removed under reduced pressure and the residue was extracted with light petroleum (bp 30–60 C°) to separate soluble material from the remainder. The light petroleum extract was concentrated and distilled to give diphenylcarbodiimide; bp 85–90 C°/ 0.2 mmHg, 1.27 g, 65%.
A further development of the method by immobilization of DEAD effects an easily separable (insoluble) and non-explosive reagent in Mitsunobu reactions. The methyl azodicarboxylate reagent immobilized on polystyrene 1742 functions well in Mitsunobu reactions and gives yields comparable to those obtained with soluble DEAD. Diphenylcarbodiimide was obtained in 41% yield.
 | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 51, p. 2613, 1986 DOI: 10.1021/jo00363a046
Synthetic Communications, 7, p. 387, 1977 DOI: 10.1080/00397917708050769 |
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