36715-97-6

Usage

Uses

Used in Pharmaceutical Industry:
3-Methyl-1,2-benzenedicarbonitrile is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the formation of complex organic molecules that possess medicinal properties.
Used in Dye Industry:
In the dye industry, 3-Methyl-1,2-benzenedicarbonitrile is utilized as a precursor in the production of dyes, where its chemical structure allows for the creation of colorants with specific characteristics.
Used in Industrial Chemicals Production:
3-Methyl-1,2-benzenedicarbonitrile is employed as a building block in the synthesis of a range of industrial chemicals, leveraging its reactivity and structural features to produce compounds with diverse applications.
It is important to handle 3-Methyl-1,2-benzenedicarbonitrile with care due to its toxic nature and potential to cause harm if not properly managed during its use in these applications.

InChI:InChI=1/C9H6N2/c1-7-3-2-4-8(5-10)9(7)6-11/h2-4H,1H3

Upstream product

• 56043-01-7 2-amino-6-methylbenzonitrile 
• 1071-98-3 2-butynedinitrile 
• 100-84-5 1-methoxy-3-methyl-benzene 
• 557-21-1 dicyanozinc 
• 143-33-9 sodium cyanide 
• 488-17-5 3-methylbenzene-1,2-diol 
• 1885-76-3 2-cyano-3-nitrotoluene 

Downstream Products

• 7251-82-3 3-Methylphthalimide 

Relevant academic research and scientific papers

An easy route from catechols to phthalonitriles

An easy synthetic route from substituted catechols via their corresponding aryl bistriflates to substituted phthalonitriles is described. The displacement of the triflate groups in catechol triflates by cyanide ions proceeded in high yields using zinc cyanide and palladium-1,1′-bis(diphenylphosphino)ferrocene as catalyst. The mild reaction conditions tolerate numerous functional groups and represent a desirable alternative to the generally low-yielding Rosenmund-von Braun reaction.

Nucleophilic addition and substitution reactions between the cyanide ion and cyclopentadienyliron complexes of chlorobenzenes. Synthesis of benzonitriles and phthalonitriles

Reaction of cyclopentadienyliron (CpFe) complexes of chlorobenzenes with NaCN in DMF could give risemto products resulting from the addition of the cyanide ion or from substitution and addition reactions with the cyanide ion.Demetallation-oxidation of such products by treatment with DDQ would lead to the synthesis of benzonitriles and phthalonitriles.With the CpFe complex of chlorobenzene, reaction with NaCN in DMF for 3 min, 30 min, or 3 h gave rise to an approximately 90:10 mixture of (1-5-η5-1-chloro-exo-6-cyanocyclohexadienyl)(η5-cyclopentadienyl)iron (9) and (1-5-η5-1-exo-6-dicyanocyclohexadienyl)(η5-cyclopentadienyl)iron (10), a 40:60 mixture of 9 and 10 or pure 10, respectively.When the 3-h reaction was worked up in the presence of an added aqueous solution of NH4PF6, only the substitution product, the (η6-benzonitrile)(η5-cyclopentadienyl)iron cation (11), was obtained as its hexafluorophosphate.Apparently, under the acidic conditions of the added aqueous NH4PF6, 10 could readily revert to 11 which gave rise to its hexafluorophosphate.DDQ treatment of the 3-min or 3-h reaction product gave, respectively, o-chlorobenzonitrile or phthalonitrile.Similary reaction of CpFe complexes of o-substituted chlorobenzenes could give rise to CpFe-complexed cyclohexadienyl systems two cyano groups,at the 1- and 6-positions and the original o-substituent at the 2-position.DDQ treatment of such products would lead to the of 3-substituted phthalonitriles, and in the present work, 3-methyl, 3-methoxy-, and 3-phenoxyphthalonitriles were prepared in this way.In another set of reactions, depending on the experimental conditions employed, the CpFe complex of 2,6-dichlorotoluene (20) could give products from cyanide addition only, the DDQ treatment of which lead to the formation of 2,4-dichloro-3-methylbenzonitrile, or products from substitution and addition and subsequent DDQ treatment of which give rise to 4-chloro-3-methylphthalonitrile.Keywords: η6-chlorobenzene-η5-cyclopentadienyliron cation, complexed chlorobenzenes, nucleophilic addition of cyanide ion, nucleophilic substitution with cyanide ion, synthesis of benzonitriles and phthalonitriles.