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269411-71-4

269411-71-4 Structure

269411-71-4 Structure
IdentificationBack Directory
[Name]

Benzonitrile, 3-amino-5-methoxy- (9CI)
[CAS]

269411-71-4
[Synonyms]

3-aMino-5-Methoxybenzonitrile
Benzonitrile,3-aMino-5-Methoxy-
Benzonitrile, 3-amino-5-methoxy- (9CI)
[Molecular Formula]

C8H8N2O
[MDL Number]

MFCD18389726
[MOL File]

269411-71-4.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

81-85 °C
[Boiling point ]

322.6±27.0 °C(Predicted)
[density ]

1.17±0.1 g/cm3(Predicted)
[storage temp. ]

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

2.37±0.10(Predicted)
[Appearance]

Light yellow to brown Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Benzonitrile, 3-amino-5-methoxy- (9CI)(269411-71-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-methoxy-5-nitrobenzonitrile

33224-19-0

Benzonitrile, 3-amino-5-methoxy- (9CI)

269411-71-4

In a three-necked flask, 3-methoxy-5-nitrobenzonitrile (8.0 g, 0.045 mol) was dissolved in methanol (80 mL), 10% palladium-carbon catalyst (1.4 g) and ammonium acetate (6.9 g, 0.090 mol) were added. Hydrogen was introduced and the reaction was stirred at 40 °C for 8 hours. After completion of the reaction, filtration was carried out and the filter cake was washed with methanol (15 mL x 3). The filtrates were combined and concentrated under reduced pressure. The concentrate was poured into 50 mL of water and extracted with ethyl acetate (40 mL x 3). The organic phases were combined, dried with anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure to give 3-amino-5-methoxybenzonitrile as a solid 6.5 g in 98.2% yield.

[References]

[1] Patent: CN107573264, 2018, A. Location in patent: Paragraph 0023-0025; 0040-0042; 0057-0059; 0074-0076
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