ChemicalBook--->CAS DataBase List--->72115-06-1

72115-06-1

72115-06-1 Structure

72115-06-1 Structure
IdentificationBack Directory
[Name]

4-amino-2-methylbenzonitrile
[CAS]

72115-06-1
[Synonyms]

4-amino-2-methylbenzonitrile
Benzonitrile, 4-amino-2-methyl-
[Molecular Formula]

C8H8N2
[MDL Number]

MFCD09260793
[MOL File]

72115-06-1.mol
[Molecular Weight]

132.16
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[Appearance]

Brown to black Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P305+P351+P338
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

4-amino-2-methylbenzonitrile(72115-06-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-METHYL-4-NITROBENZONITRILE  98

89001-53-6

4-amino-2-methylbenzonitrile

72115-06-1

(b) Synthesis of 4-amino-2-methylbenzonitrile: Tin chloride dihydrate (18.5 g, 82.0 mmol) was added to a solution of 2-methyl-4-nitrobenzonitrile (3.80 g, 23.4 mmol) in ethanol (140 mL). The reaction mixture was stirred under reflux conditions for 3 hours. After completion of the reaction, the solvent was removed by distillation. The residue was diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate solution. The precipitate produced during washing was removed by filtration through diatomaceous earth. The filtrate was extracted with ethyl acetate and the combined organic phases were dried with anhydrous magnesium sulfate, filtered and concentrated to give 4-amino-2-methylbenzonitrile (2.89 g, 94% yield).

[References]

[1] Patent: EP1500643, 2005, A1. Location in patent: Page 32
[2] Chemische Berichte, 1919, vol. 52, p. 1083
[3] Journal of Organic Chemistry, 1962, vol. 27, p. 1426 - 1430
[4] Journal of Medicinal Chemistry, 2001, vol. 44, # 23, p. 3856 - 3871
[5] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 6, p. 1926 - 1930
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