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38803-30-4

38803-30-4 Structure

38803-30-4 Structure
IdentificationBack Directory
[Name]

3-(Dimethylamino)benzonitrile
[CAS]

38803-30-4
[Synonyms]

3-(Dimethylamino)benzonitrile
Benzonitrile, 3-(dimethylamino)-
[Molecular Formula]

C9H10N2
[MDL Number]

MFCD00159008
[MOL File]

38803-30-4.mol
[Molecular Weight]

146.19
Chemical PropertiesBack Directory
[Melting point ]

27 °C
[Boiling point ]

148-149 °C(Press: 14 Torr)
[density ]

1.04±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

3.02±0.10(Predicted)
[Appearance]

Light yellow to brown <27°C Solid,>27°C Liquid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H317
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
[HS Code ]

2922390090
Spectrum DetailBack Directory
[Spectrum Detail]

3-(Dimethylamino)benzonitrile(38803-30-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Formaldehyde

50-00-0

3-Aminobenzonitrile

2237-30-1

3-(Dimethylamino)benzonitrile

38803-30-4

To a solution of m-aminobenzonitrile (1.0 g, 8.5 mmol) and formaldehyde (2.1 g, 69.0 mmol) in acetonitrile (20 mL) was added sodium cyanoborohydride (2.7 g, 42.5 mmol). The reaction mixture was stirred at room temperature for 2 hours. Acetic acid (100 mL) was added to adjust the pH to 7 and stirring was continued for 2 hours. Potassium hydroxide solution (1N, 100 mL) was then added and the mixture was extracted with ethyl acetate (100 mL x 2). The organic layers were combined, washed with saturated saline (80 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with petroleum ether/ethyl acetate (10:1) as eluent to give 3-(dimethylamino)benzonitrile (1.3 g, 100%) as a colorless oil. Mass spectrum (MS): m/z 147.3 ([M+H]+).

[References]

[1] Patent: WO2018/132372, 2018, A1. Location in patent: Paragraph 00470
[2] Bioorganic and Medicinal Chemistry Letters, 1996, vol. 6, # 5, p. 565 - 568
[3] European Journal of Medicinal Chemistry, 1998, vol. 33, # 5, p. 363 - 374
[4] Journal of Chemical Physics, 1988, vol. 88, # 2, p. 871 - 878
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