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Chemical Structure| 870-85-9 Chemical Structure| 870-85-9

Structure of 870-85-9

Chemical Structure| 870-85-9

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Product Details of [ 870-85-9 ]

CAS No. :870-85-9
Formula : C7H13NO2
M.W : 143.18
SMILES Code : C/C(NC)=C\C(OCC)=O
MDL No. :MFCD00026904

Safety of [ 870-85-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 870-85-9 ]

* 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 [ 870-85-9 ]

[ 870-85-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 870-85-9 ]
  • [ 67-64-1 ]
  • [ 106-51-4 ]
  • [ 15574-49-9 ]
  • 2
  • [ 870-85-9 ]
  • [ 106-51-4 ]
  • [ 15574-49-9 ]
YieldReaction ConditionsOperation in experiment
74.9% In 1,2-dichloro-ethane; at 50℃; for 12.0h;Reflux; P-benzoquinone (9.1 g, 83.81 mmol) was dissolved in 1,2-dichloroethane and heated to 50 C.Then a solution of Intermediate 2 (10.0 g, 69.84 mmol) in 1,2-dichloroethane was slowly added dropwise.After the completion of the dropwise addition, the reflux reaction was continued for 12 hours, and the reaction was completed by TLC, and the solid was washed off by cooling.Filtration was carried out to obtain 12.2 g of Intermediate 3 in a yield of 74.9%.
73.7% In acetone; at 30℃; for 2.0h; General procedure: Synthetic method: A mixture of p-benzoquinone (11.89 g, 0.11 mol) And acetone 120mL Placed in 250mL eggplant bottle, A solution of 0.11 mol of the intermediate 3-substituted amino-2-butenoic acid ethyl ester was added dropwise with stirring, After the drop control temperature 30 to continue reaction 2h, The solvent was distilled off and the crude product was recrystallized from acetone.
73.7% In acetone; at 30℃; for 2.0h; p-benzoquinone (11.89g, 0.11mol) and acetone 120mL were placed in a 250mL eggplant-shaped flask, and 0.11mol of 3-methylamino-2-butenoic acid ethyl ester was added dropwise with stirring. After the addition was completed, the temperature was controlled at 30 C. continue reaction 2h. The solvent was distilled off, the crude product was recrystallized from acetone to give a white colored solid 18.92g, yield: 73.7%.
  • 3
  • [ 1072-87-3 ]
  • [ 870-85-9 ]
  • [ 80049-31-6 ]
  • 4
  • [ 870-85-9 ]
  • [ 637-88-7 ]
  • [ 15574-49-9 ]
YieldReaction ConditionsOperation in experiment
In 1,2-dichloro-ethane; for 8.0h;Reflux; General procedure: The p-benzoquinone (0.096 mol) was dissolved in 100 mL of 1,2-dichloroethane, heated to 60 C., stirred until dissolution was complete, compound A-1 was added dropwise, and the reaction was completed by refluxing for 8 h.The reaction solution was allowed to naturally cool to room temperature and allowed to stand overnight to precipitate a solid, which was filtered by suction, washed with cold acetone, dried, and recrystallized from acetone to obtain compound A-2. Yield: 40-60%.
 

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