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N-(2-Cyanoethyl)-N-methylaniline

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N-(2-Cyanoethyl)-N-methylaniline Basic information

Product Name:
N-(2-Cyanoethyl)-N-methylaniline
Synonyms:
  • 3-(methylphenylamino)-propanenitril
  • N-Methyl-N-Cyanoethyl Aniline
  • 3-(methyl(phenyl)amino)propanenitrile
  • 3-(METHYLPHENYLAMINO)PROPIONITRILE 97%
  • N-(2-CYANOETHYL)-N-METHYLANILINE / 3-(METHYLPHENYLAMINO)PROPIONITRILE
  • 3-(N-Methyl-N-phenylamino)propiononitrile
  • 3-(N-methylanilino)propanenitrile
  • N-Methyl-N-(2-cyanoethyl)aniline 3-(N-Methyl-N-phenylamino)propionitrile
CAS:
94-34-8
MF:
C10H12N2
MW:
160.22
EINECS:
202-325-5
Product Categories:
  • aniline derivatives
  • Intermediates of Dyes and Pigments
Mol File:
94-34-8.mol
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N-(2-Cyanoethyl)-N-methylaniline Chemical Properties

Boiling point:
313 °C(lit.)
Density 
1.035 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.56(lit.)
Flash point:
125-127°C/4mm
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
pka
4.54±0.50(Predicted)
color 
White to Yellow to Green
Specific Gravity
1.05
BRN 
2803416
CAS DataBase Reference
94-34-8(CAS DataBase Reference)
EPA Substance Registry System
Propanenitrile, 3-(methylphenylamino)- (94-34-8)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-21/22
Safety Statements 
26-36-36/37
WGK Germany 
3
TSCA 
Yes
PackingGroup 
III
HS Code 
29214300

MSDS

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N-(2-Cyanoethyl)-N-methylaniline Usage And Synthesis

Synthesis

An activated carbon-supported platinum catalyst (Pt / C, 0.06 mg platinum, 0.0003 mmol, 0.1 mol percent) was added to a 10 mL Schlenk tube; after the evacuation of argon, add 1 mL of solvent (toluene). Under argon protection, to the above system, Were successively added phenylsilane (78.9 mg, 0.75 mmol), 3-Anilinopropionitrile (43.9 mg, 0.3 mmol) and formic acid (27.6 mg, 0.6 mmol). The whole anti-reaction was carried out at 80 ° C with stirring for 15 hours. After completion of the reaction, 3 mL of ethyl acetate was added to the system. The reaction was quenched with aqueous sodium hydroxide (3 mol / L, 3 mL). Ethyl acetate (3 x 10 mL), the organic phase was separated, Dried over anhydrous Na2SO4, and filtered; the solvent was removed by rotary evaporation. The residue was purified by column chromatography on ethyl acetate/petroleum ether = 1: 50 mixed solvent. Separation and purification gave N-(2-Cyanoethyl)-N-methyl aniline 226.4 mg, yield of 55 per cent.

N-(2-Cyanoethyl)-N-methylaniline Preparation Products And Raw materials

Preparation Products

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