The Kirsanov reaction is a method for the synthesis of certain organophosphorus compounds. In this reaction a tertiary phosphine is combined with a halogen and then an amine to give the iminophosphines, which are useful ligands and useful reagents. [1] A typical reaction involves triphenylphosphine with bromine to give bromotriphenyl phosphonium bromide:
- Ph3P + Br2 → Ph3PBr+Br−
This salt is treated in situ with alkylamines to give the iminophosphorane:
- Ph3PBr+Br− + 3 RNH2 → Ph3PNR + 2 RNH3+Br−
The method is used when the conventional Staudinger reaction is not applicable, i.e. when the organic azide is not available to generate the iminophosphorane. Thus, it is used to make iminophosphoranes from alkyl amines. [2]
- ^ Eguchi, Shoji; Matsushita, Yuji; Yamashita, Keizo (April 1992). "The Aza-Wittic Reaction in Heterocyclic Synthesis. A Review". Organic Preparations and Procedures International. 24 (2): 209–243. doi: 10.1080/00304949209355702.
- ^ Buchard, Antoine; Heuclin, Hadrien; Auffrant, Audrey; Le Goff, Xavier F.; Le Floch, Pascal (2009). "Coordination of tetradentate X2N2 (X = P, S, O) ligands to iron(ii) metal center and catalytic application in the transfer hydrogenation of ketones". Dalton Transactions (9): 1659–67. doi: 10.1039/b816439h. PMID 19421611.
The Kirsanov reaction is a method for the synthesis of certain organophosphorus compounds. In this reaction a tertiary phosphine is combined with a halogen and then an amine to give the iminophosphines, which are useful ligands and useful reagents. [1] A typical reaction involves triphenylphosphine with bromine to give bromotriphenyl phosphonium bromide:
- Ph3P + Br2 → Ph3PBr+Br−
This salt is treated in situ with alkylamines to give the iminophosphorane:
- Ph3PBr+Br− + 3 RNH2 → Ph3PNR + 2 RNH3+Br−
The method is used when the conventional Staudinger reaction is not applicable, i.e. when the organic azide is not available to generate the iminophosphorane. Thus, it is used to make iminophosphoranes from alkyl amines. [2]
- ^ Eguchi, Shoji; Matsushita, Yuji; Yamashita, Keizo (April 1992). "The Aza-Wittic Reaction in Heterocyclic Synthesis. A Review". Organic Preparations and Procedures International. 24 (2): 209–243. doi: 10.1080/00304949209355702.
- ^ Buchard, Antoine; Heuclin, Hadrien; Auffrant, Audrey; Le Goff, Xavier F.; Le Floch, Pascal (2009). "Coordination of tetradentate X2N2 (X = P, S, O) ligands to iron(ii) metal center and catalytic application in the transfer hydrogenation of ketones". Dalton Transactions (9): 1659–67. doi: 10.1039/b816439h. PMID 19421611.