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Chemical Structure| 21759-70-6 Chemical Structure| 21759-70-6

Structure of 21759-70-6

Chemical Structure| 21759-70-6

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Product Details of [ 21759-70-6 ]

CAS No. :21759-70-6
Formula : C7H13NO2
M.W : 143.18
SMILES Code : C/C(NC)=C/C(OCC)=O
MDL No. :MFCD03060877

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Application In Synthesis of [ 21759-70-6 ]

* 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 [ 21759-70-6 ]

[ 21759-70-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 21759-70-6 ]
  • [ 106-51-4 ]
  • [ 15574-49-9 ]
YieldReaction ConditionsOperation in experiment
75.2% In acetone; at 30℃; for 2.0h; General procedure: To a solution of benzoquinone (12.40 g, 0.11 mol) in acetone (120 mL), 2a or 2b (0.11 mol) was added dropwise at 30C, and the reaction mixture was stirred at this temperature for 2 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo and the residue was purified by recrystallization with acetone to afford the product as solid. Ethyl 5-hydroxy-1,2-dimethyl-1H-indole-3-carboxylate (3a). White solid; yield: 75.2%; M.p.: 208-210C (lit.[19]: 208-209C). ESI-MS, m/z: calcd. 233.11(M+); found 234.1 ([M+H]+), 356.1([M+Na]+).
75.2% In acetone; at 30℃; for 2.0h; General procedure: To a solution of benzoquinone (12.40 g, 0.11 mol) in acetone (120 mL), 2a or 2b (0.11 mol) was added dropwise at 30 C, and the reaction mixture was stirred at this temperature for 2 h. After cooling to room temperature, the reaction mixture was concent rated in vacuo and the residue was purified by recrystallization with acetone to afford product as solid.
In 1,2-dichloro-ethane; at 20 - 60℃;Heating / reflux; To 100 mL of 1,2-dichloroethane was added 0.096 mol of 1,4-benzoquinone, and the mixture was stirred and heated to 60C. After 1,4-benzoquinone was dissolved, Compound A-1 was added dropwise to the solution and reacted under refluxing for 8h. The solution was cooled to room temperature and kept overnight. The precipitate was collected by filtration, washed with cold acetone, dried, and recrystallized from acetone to give 40-60% yield of compound A-2.
 

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