Kabachnik–Fields reaction: Difference between revisions
import errant content from Pudovik reaction and some other tweaks |
imine formation is not a mannich reaction |
||
| Line 3: | Line 3: | ||
:[[Image:Kabachnik-Fields Reaction.svg|Kabachnik-Fields Reaction]] |
:[[Image:Kabachnik-Fields Reaction.svg|Kabachnik-Fields Reaction]] |
||
The first step in this reaction is the formation of an [[imine |
The first step in this reaction is the formation of an [[imine]], followed by a [[hydrophosphonylation]] step where the phosphonate P-H bond across the C=N double bond.<ref>{{cite journal| last=Zefirov | first=Nikolay S. |author2=Elena D. Matveeva | date=2008-01-18 | title=Catalytic Kabachnik-Fields reaction: New horizons for old reaction | journal=[[ARKIVOC]] | volume=2008 | issue=i | pages=1–17 | url=http://www.arkat-usa.org/get-file/22930/?wikipedia-format=.pdf | accessdate=2009-12-08 | doi=10.3998/ark.5550190.0009.101}}</ref> The starting carbonyl component is usually an [[aldehyde]] and sometimes a [[ketone]]. The reaction can be accelerated with a combination of dehydrating reagent and [[Lewis acid]]. |
||
Enantioselective variants of the Kabachnik-Fields reaction have been developed, for example employing α-methylbenzylamine provides a chiral, non-racemic α-aminophosphonate.<ref>{{cite journal|author1=Gilmore, F. |author2=McBride, A. |journal=J. Am. Chem. Soc.|year=1972|volume=94|pages= 4361|doi=10.1021/ja00767a065|pmid=5036657|title=Synthesis of an optically active -aminophosphonic acid|issue=12}}</ref> |
Enantioselective variants of the Kabachnik-Fields reaction have been developed, for example employing α-methylbenzylamine provides a chiral, non-racemic α-aminophosphonate.<ref>{{cite journal|author1=Gilmore, F. |author2=McBride, A. |journal=J. Am. Chem. Soc.|year=1972|volume=94|pages= 4361|doi=10.1021/ja00767a065|pmid=5036657|title=Synthesis of an optically active -aminophosphonic acid|issue=12}}</ref> |
||
Revision as of 19:40, 27 April 2019
In organophosphorus chemistry, the Kabachnik–Fields reaction is a three-component organic reaction forming α-aminomethylphosphonates from an amine, a carbonyl compound, and a dialkyl phosphonate, (RO)2P(O)H (that are also called dialkylphosphites).[1] Aminophosphonates are synthetic targets of some importance as phosphorus analogues of α-amino acids (a bioisostere). This multicomponent reaction was independently discovered by Martin Izrailevich Kabachnik[2] and Ellis K. Fields[3] in 1952. The reaction is very similar to the two-component Pudovik reaction, which involves condensation of the phosphite and a preformed imine.
The first step in this reaction is the formation of an imine, followed by a hydrophosphonylation step where the phosphonate P-H bond across the C=N double bond.[4] The starting carbonyl component is usually an aldehyde and sometimes a ketone. The reaction can be accelerated with a combination of dehydrating reagent and Lewis acid.
Enantioselective variants of the Kabachnik-Fields reaction have been developed, for example employing α-methylbenzylamine provides a chiral, non-racemic α-aminophosphonate.[5]
References
- ^ "The Kabachnik-Fields reaction: mechanism and synthetic use". Molecules. 17: 12821–12835. 2012. doi:10.3390/molecules171112821.
{{cite journal}}: Unknown parameter|authors=ignored (help)CS1 maint: unflagged free DOI (link) - ^ Kabachnik, Martin I.; Medved, T. Ya. (1952). "Новый метод синтеза сс-аминофосфиновых кислот" [A new method for the synthesis of α-amino phosphoric acids]. Doklady Akademii Nauk SSSR (in Russian). 83: 689ff.
- ^ Fields, Ellis K. (1952). "The synthesis of esters of substituted amino phosphonic acids". Journal of the American Chemical Society. 74 (6): 1528–1531. doi:10.1021/ja01126a054.
- ^ Zefirov, Nikolay S.; Elena D. Matveeva (2008-01-18). "Catalytic Kabachnik-Fields reaction: New horizons for old reaction" (PDF). ARKIVOC. 2008 (i): 1–17. doi:10.3998/ark.5550190.0009.101. Retrieved 2009-12-08.
- ^ Gilmore, F.; McBride, A. (1972). "Synthesis of an optically active -aminophosphonic acid". J. Am. Chem. Soc. 94 (12): 4361. doi:10.1021/ja00767a065. PMID 5036657.