Benzophenone imine

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Benzophenone imine
Benzophenone imine.svg
Names
Preferred IUPAC name
Diphenylmethanimine
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.103.715 Edit this at Wikidata
EC Number
  • 600-205-0
  • 440-870-2
UNII
  • InChI=1S/C13H11N/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,14H
    Key: SXZIXHOMFPUIRK-UHFFFAOYSA-N
  • C1=CC=C(C=C1)C(=N)C2=CC=CC=C2
Properties
C13H11N
Molar mass 181.238 g·mol−1
Hazards
GHS labelling:
GHS07: Exclamation mark
Signal word
 Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Benzophenone imine is an organic compound with the formula of (C6H5)2C=NH. Benzophenone imine is widely used as a reagent for the protection of primary amines and as an ammonia synthon in cross-coupling reactions to prepare anilines.[1]

Synthesis[]

Benzophenone imine is prepared by the reaction of benzonitrile and phenyl Grignard or by the condensation of benzophenone and ammonia.

Synthesis by Grignard-nitrile complexes[]

Synthesis of benzophenone imine assisted by grignard reagent[2]

The first report about the preparation of ketimines involved Grignard-nitrile complexes followed by careful hydrolysis, which is known as Moureu-Mignonac ketimine synthesis.[3] Then Pickard and Tolbert improved the preparation by using methanol in the addition of Grignard-nitrile complexes.[2]

Synthesis by benzophenone and ammonia[]

In 1988, A. G. Guimanini discovered a new route to synthesize benzophenone imine by a reaction using benzophenone and ammonia. A chemical pure-grade ammonia gas is added to a benzophenone solution, forming Ph2C=NH2+. After sodium hydroxide pellets are added to the solution, the Ph2C=NH2+ is neutralized, generating the expected benzophenone imine.[4]

Applications[]

Protecting group for primary amines[]

Primary amines can be protected benzophenone imine, and the protected amines are stable in flash chromatography.[5]

Amination of aryl halides[]

Buchwald-Hartwig amination is a very important kind of reaction for coupling aromatic halide and amine to form carbon-nitrogen bonds with the help of palladium-involved catalysts. In order to obtain anilines, ammonia is required in this reaction. However, ammonia can bind to palladium tightly, which makes the normal Buchwald-Hartwig reaction unavailable. In 1997, Buchwald et. al found that benzophenone imine can be used as an ammonia-equivalent and solve the above limitations.[1]

Palladium-catalyzed amination of aryl halides via benzophenone imine[1]

References[]

  1. ^ a b c Wolfe, John P.; Åhman, Jens; Sadighi, Joseph P.; Singer, Robert A.; Buchwald, Stephen L. (1997-09-08). "An Ammonia Equivalent for the Palladium-Catalyzed Amination of Aryl Halides and Triflates". Tetrahedron Letters. 38 (36): 6367–6370. doi:10.1016/S0040-4039(97)01465-2. ISSN 0040-4039.
  2. ^ a b Pickard, P. L.; Tolbert, T. L. (December 1961). "An Improved Method of Ketimine Synthesis". The Journal of Organic Chemistry. 26 (12): 4886–4888. doi:10.1021/jo01070a025. ISSN 0022-3263.
  3. ^ Moureau-Mignonac Ketimine Synthesis. Comprehensive Organic Name Reactions and Reagents. Hoboken, NJ, USA: John Wiley & Sons, Inc. 2010-09-15. pp. 1988–1990. doi:10.1002/9780470638859.conrr446. ISBN 9780470638859.
  4. ^ Verardo, G.; Giumanini, A. G.; Strazzolini, P.; Poiana, M. (1988). "Ketimines From Ketones and Ammonia". Synthetic Communications. 18 (13): 1501–1511. doi:10.1080/00397918808081307.
  5. ^ O'Donnell, Martin J. (2001-04-15). Benzophenone Imine. Encyclopedia of Reagents for Organic Synthesis. Chichester, UK: John Wiley & Sons, Ltd. doi:10.1002/047084289x.rb031. ISBN 978-0471936237.
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