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Chemical Structure| 96-16-2 Chemical Structure| 96-16-2

Structure of 96-16-2

Chemical Structure| 96-16-2

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Product Details of [ 96-16-2 ]

CAS No. :96-16-2
Formula : C4H8N2
M.W : 84.11
SMILES Code : N#CC(C)CN
English Name :3-Amino-2-methylpropanenitrile
MDL No. :MFCD11651462

Safety of [ 96-16-2 ]

Application In Synthesis of [ 96-16-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 96-16-2 ]

[ 96-16-2 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 126-98-7 ]
  • [ 96-16-2 ]
YieldReaction ConditionsOperation in experiment
With ammonia; water at 135℃;
With ammonium hydroxide at 135℃; for 3h; 16 3-amino-2-methyl-propanenitrile The solution of 2-methylprop-2-enenitrile (2 g, 29.81 mmol, 2.50 mL, 1 eq) in NH3.H2O (9.1 g, 72.71 mmol, 10 mL, 28% purity, 2.44 eq) was stirred for 3 hr at 135 °C (no monitor). The reaction mixture was cooled to 15 °C. Then distilled at 130 °C to give the crude product. The crude product was concentrated in vacuo for 0.5 hr at 0 °C to remove the remaining NH3.H2O to afford the title compound 3-amino-2-methyl-propanenitrile (0.2 g, crude) as a colorless liquid which was used for the next step directly without further purification.
With ammonium hydroxide at 135℃; for 3h; 16 3-amino-2-methyl-propanenitrile The solution of 2-methylprop-2-enenitrile (2 g, 29.81 mmol, 2.50 mL, 1 eq) in NH3.H2O (9.1 g, 72.71 mmol, 10 mL, 28% purity, 2.44 eq) was stirred for 3 hr at 135 °C (no monitor). The reaction mixture was cooled to 15 °C. Then distilled at 130 °C to give the crude product. The crude product was concentrated in vacuo for 0.5 hr at 0 °C to remove the remaining NH3.H2O to afford the title compound 3-amino-2-methyl-propanenitrile (0.2 g, crude) as a colorless liquid which was used for the next step directly without further purification.
  • 3
  • [ 96-16-2 ]
  • [ CAS Unavailable ]
  • [ 741616-85-3 ]
YieldReaction ConditionsOperation in experiment
In 1,4-dioxane
  • 4
  • [ 96-16-2 ]
  • [ 16750-44-0 ]
YieldReaction ConditionsOperation in experiment
With hydroxylamine hydrochloride
  • 6
  • [ 96-16-2 ]
  • [ 4016-85-7 ]
  • [ 59049-58-0 ]
YieldReaction ConditionsOperation in experiment
In 1,4-dioxane
  • 7
  • [ 96-16-2 ]
  • [ 6021-21-2 ]
  • [ 786582-34-1 ]
YieldReaction ConditionsOperation in experiment
In 1,4-dioxane
  • 8
  • [ 96-16-2 ]
  • [ CAS Unavailable ]
  • [ 120241-52-3 ]
YieldReaction ConditionsOperation in experiment
98% In ethanol 7 N-(2-Cyanoethyl)-2-methyl-3-aminopropionitrile (10) EXAMPLE 7 N-(2-Cyanoethyl)-2-methyl-3-aminopropionitrile (10) A solution of 2-methyl-3-aminopropionitrile (9)2 (197 g, 2.35 mol) and acrylonitrile (170 ml) in ethanol (250 ml) was refluxed overnight and then evaporated in vacuo to yield 10 (316 g, 98%) as a light oil.
98% In ethanol 35 N-(2-Cyanoethyl)-2-methyl-3-aminopropionitrile (41) EXAMPLE 35 N-(2-Cyanoethyl)-2-methyl-3-aminopropionitrile (41) A solution of 2-methyl-3-aminopropionitrile (40) (Eastman Kodak Co., U.S. Pat. No. 2,659,739 (1950)) (197 g, 2.35 mol) and acrylonitrile (170 ml) in ethanol (250 ml) was refluxed overnight and then evaporated in vacuo to yield 41 (316 g, 98%) as a light oil.
95.3% In ethanol for 16h; Heating;
YieldReaction ConditionsOperation in experiment
Oxid. mit H2O2;
YieldReaction ConditionsOperation in experiment
Methacrylonitril, 40percentig.wss.NH3, 100grad (Autoklav);
NH3, Methacrylsaeure (140grad);
Methacrylonitril, 28percentig. wss. NH3/70-75grad;
 

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