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Chemical Structure| 1037301-15-7 Chemical Structure| 1037301-15-7

Structure of 1037301-15-7

Chemical Structure| 1037301-15-7

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Product Details of [ 1037301-15-7 ]

CAS No. :1037301-15-7
Formula : C5H8N2O
M.W : 112.13
SMILES Code : N#CC1(N)COCC1
MDL No. :MFCD18333627

Safety of [ 1037301-15-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1037301-15-7 ]

* 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 [ 1037301-15-7 ]

[ 1037301-15-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22929-52-8 ]
  • potassium cyanide [ No CAS ]
  • [ 1037301-15-7 ]
YieldReaction ConditionsOperation in experiment
With ammonia; acetic acid; In methanol; at 0 - 50℃; for 2h; 0183] Step 3: To a solution of <strong>[22929-52-8]dihydrofuran-3(2H)-one</strong> (10.0 g, 116 mmol) in ammonia (solution in methanol, 100 mL) at 0°C was added acetic acid (7.67 g, 128 mmol) followed by potassium cyanide (7.56 g, 116 mmol). The reaction mixture was heated to 50°C. After 2 hours, the reaction mixture was cooled to ambient temperature and concentrated under reduced pressure to afford the crude residue. The residue was diluted with aqueous iron sulfate (100 mL) and extracted with ethyl acetate (3 x 20 mL). The organics were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 3-aminotetrahydrofuran-3-carbonitrile. The material was used without purification.
With ammonia; acetic acid; In methanol; at 0 - 50℃; for 2h; To a solution of <strong>[22929-52-8]dihydrofuran-3(2H)-one</strong> (10.0 g, 116 mmol) in ammonia (solution in methanol, 100 mL) at 0°C was added acetic acid (7.67 g, 128 mmol) followed by potassium cyanide (7.56 g, 1 16 mmol). The reaction mixture was heated to 50°C. After 2 hours, the reaction mixture was cooled to ambient temperature and concentrated under reduced pressure to afford the crude residue. The residue was diluted with aqueous iron sulfate (100 mL) and extracted with ethyl acetate (3 x 20 mL). The organics were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 3-aminotetrahydrofuran-3- carbonitrile. The material was used without purification.
 

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