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Chemical Structure| 146335-23-1 Chemical Structure| 146335-23-1

Structure of 146335-23-1

Chemical Structure| 146335-23-1

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Product Details of [ 146335-23-1 ]

CAS No. :146335-23-1
Formula : C9H9NO2
M.W : 163.17
SMILES Code : OCC1=CC(CO)=CC(C#N)=C1

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Application In Synthesis of [ 146335-23-1 ]

* 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 [ 146335-23-1 ]

[ 146335-23-1 ] Synthesis Path-Downstream   1~3

  • 1
  • CCuN*CNNa [ No CAS ]
  • [ 71176-54-0 ]
  • [ 146335-23-1 ]
  • 2
  • [ 71176-54-0 ]
  • Cu2(CN)2 [ No CAS ]
  • [ 146335-23-1 ]
  • 3
  • [ 773837-37-9 ]
  • copper(l) cyanide [ No CAS ]
  • [ 71176-54-0 ]
  • [ 146335-23-1 ]
YieldReaction ConditionsOperation in experiment
41% A solution of 26 (5 g, 33 mmol) in 2N hydrochloric acid (100 mL) was cooled to 0°C and treated with a cold solution of sodium nitrite (3.53 g, 36mmol) in water (50 mL). The reaction mixture was maintained at a temperature < 5°C for 30min then treated with a solution of copper(I) cyanide (3.19 g, 35.6mmol) and sodium cyanide (3.53 g, 72mmol) in water (50 mL) in a single portion. After stirring overnight at room temperature the mixture was filtered, extracted with dichloromethane (3 x 100 mL), concentrated and used without further purification. The diol, 3,5-bis(hydroxymethyl)benzonitrile 27 was obtained as a yellow solid (2.19 g, 41percent). Rf 0.75 (15percent MeOH-CH2Cl2).
41% A solution of 26 (5 g, 33 mmol) in 2N hydrochloric acid (100 mL) was cooled to 0°C and treated with a cold solution of sodium nitrite (3.53 g, 36mmol) in water (50 mL). The reaction mixture was maintained at a temperature < 5°C for 30min then treated with a solution of copper(I) cyanide (3.19 g, 35.6mmol) and sodium cyanide (3.53 g, 72mmol) in water (50 mL) in a single portion. After stirring overnight at room temperature the mixture was filtered, extracted with dichlorom ethane (3 x 100 mL), concentrated and used without further purification. The diol, 3,5-bis(hydroxymethyl)benzonitrile 27 was obtained as a yellow solid (2.19 g, 41percent). Rf 0.75 (15percent MeOH-CH2Cl2).
41% A solution of 26 (5 g, 33 mmol) in 2N hydrochloric acid (100 mL) was cooled to 0°C and treated with a cold solution of sodium nitrite (3.53 g, 36mmol) in water (50 mL). The reaction mixture was maintained at a temperature < 5°C for 30min then treated with a solution of copper(I) cyanide (3.19 g, 35.6mmol) and sodium cyanide (3.53 g, 72mmol) in water (50 mL) in a single portion. After stirring overnight at room temperature the mixture was filtered, extracted with dichlorom ethane (3 x 100 mL), concentrated and used without further purification. The diol, 3,5-bis(hydroxymethyl)benzonitrile 27 was obtained as a yellow solid (2.19 g, 41percent). Rf 0.75 (15percent MeOH-CH2Cl2).
 

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