Editing Pinner reaction

{{Short description|Reaction of cyanide and alcohol to give imino ester salt}}
{{Reactionbox
| Name = Pinner reaction
| NamedAfter = [[Adolf Pinner]]
| Section3 = {{Reactionbox Identifiers
   | OrganicChemistryNamed = pinner-reaction
   | RSC_ontology_id = 0000361
 }}
}}
The '''Pinner reaction''' refers to the acid catalysed reaction of a [[nitrile]] with an [[Alcohol (chemistry)|alcohol]] to form an imino ester salt ([[alkyl]] [[imidate]] salt); this is sometimes referred to as a '''Pinner salt'''.<ref>{{cite journal|title=Pinner Reaction|journal = Comprehensive Organic Name Reactions and Reagents|year=2010|issue = 504 | pages = 2237–2240 |doi=10.1002/9780470638859.conrr504|isbn = 9780470638859}}</ref>
The reaction is named after [[Adolf Pinner]], who first described it in 1877.<ref>{{cite journal 
 | title =  Umwandlung der Nitrile in Imide  | author = A. Pinner, F. Klein  | journal = [[Berichte der deutschen chemischen Gesellschaft]]  
 | volume = 10  | issue = 2 | pages = 1889–1897 | year = 1877  | url =   https://zenodo.org/record/1425138| doi = 10.1002/cber.187701002154   | last2 = Klein  }}</ref><ref>{{cite journal  | title = Umwandlung der Nitrile in Imide   | author = A. Pinner, Fr. Klein   | journal =  [[Berichte der deutschen chemischen Gesellschaft]]   | volume = 11    | issue = 2 | pages = 1475–1487  | year = 1878  | url =   https://zenodo.org/record/1425138| doi = 10.1002/cber.18780110258   | last2 = Klein  
 }}</ref><ref>{{cite journal  | title = Ueber die Umwandlung der Nitrile in Imide   | author =  A. Pinner  | journal =  [[Berichte der deutschen chemischen Gesellschaft]]   | volume = 16  | issue = 2 | pages = 1643–1655  | year = 1883  | url =  https://zenodo.org/record/1425307| doi = 10.1002/cber.18830160235}}</ref>
Pinner salts are themselves reactive and undergo additional [[nucleophilic addition]]s to give various useful products:<ref>{{cite journal | last1 = Roger | first1 = R. | last2 = Neilson | first2 = D. G. | year = 1961 | title =  The Chemistry of Imidates| journal = [[Chem. Rev.]] | volume = 61 | issue = 2| pages = 179–211 | doi = 10.1021/cr60210a003 }}</ref><ref>{{cite journal|last1=Adams|first1=Roger|last2=Thal|first2=A. F.|title=Ethyl Phenylacetate|journal=[[Organic Syntheses]]|date=1922|volume=2|page=27|doi=10.15227/orgsyn.002.0027}}</ref>
* With an excess of alcohol to form an [[orthoester]] 
* With [[ammonia]] or an [[amine]] to form an [[amidine]] (di-nitriles may form [[imidine]]s, for instance succinimidine from [[succinonitrile]])<ref>{{cite journal |last1=Elvidge |first1=J. A. |last2=Linstead |first2=R. P. |title=Heterocyclic imines and amines. Part III. Succinimidine |journal=Journal of the Chemical Society (Resumed) |date=1954 |pages=442 |doi=10.1039/JR9540000442}}</ref>
* With water to form an [[ester]]
* With [[hydrogen sulfide]] to form a [[thionoester]]
[[Image:Reaction-pinner2.png|center]]
Commonly, the Pinner salt itself is not isolated, with the reaction being continued to give the desired functional group (orthoester etc.) in one go. The imidium chloride salt is thermodynamically unstable, and low temperatures help prevent elimination to an [[amide]] and [[alkyl chloride]].<ref>{{cite book|page=5|title=Carboxylic Ortho Acid Derivatives|series=Organic Chemistry|volume=14|first=Robert&nbsp;H.|last=DeWolfe|year=1970|publisher=Academic Press|location=New York, NY|lccn=70-84226}}</ref>  

It should be appreciated that the Pinner reaction refers specifically to an acid catalyzed process, but that similar results can often be achieved using base catalysis. The two approaches can be complementary, with nitriles which are unreactive under acid conditions often giving better results in the presence of base, and vice versa.<ref>{{Cite journal | doi = 10.1021/jo01061a034| title = Base-Catalyzed Reaction of Nitriles with Alcohols. A Convenient Route to Imidates and Amidine Salts| journal = [[Journal of Organic Chemistry]] | volume = 26| issue = 2| pages = 412| year = 1961| last1 = Schaefer | first1 = F. C. | last2 = Peters | first2 = G. A. }}</ref> The determining factor is typically how electron-rich or poor the nitrile is. For example: an electron-poor nitrile is a good electrophile (readily susceptible to attack from [[alkoxide]]s etc.) but a poor nucleophile would typically be easier to protonate than to participate in the reaction and hence would be expected to react more readily under basic rather than acidic conditions.

==See also==
* [[Hoesch reaction]]
* [[Overman rearrangement]]
* [[Isocyanide]]
* [[Imidoyl chloride]]
* [[Stephen aldehyde synthesis]] – essentially the same reaction but including a [[Organic redox reaction|reduction]] and with water as the nucleophile; generates the aldehyde.

==References==
{{Reflist}}

{{DEFAULTSORT:Pinner Reaction}}
[[Category:Addition reactions]]
[[Category:Name reactions]]