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Chemical Structure| 20926-88-9 Chemical Structure| 20926-88-9

Structure of 20926-88-9

Chemical Structure| 20926-88-9

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Product Details of [ 20926-88-9 ]

CAS No. :20926-88-9
Formula : C9H5ClO2
M.W : 180.59
SMILES Code : O=C1CC(C2=C1C=CC=C2Cl)=O

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Application In Synthesis of [ 20926-88-9 ]

* 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 [ 20926-88-9 ]

[ 20926-88-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 117-21-5 ]
  • [ 141-97-9 ]
  • [ 20926-88-9 ]
YieldReaction ConditionsOperation in experiment
General procedure: To a solution of compounds 2a-2h (5 mmol) in acetic anhydride (5 mL) and triethylamine (2.5 mL) was added ethyl acetoacetate (0.71 mL, 5.5 mmol) under argon. The reaction mixture was stirred at rt for 12 h and then poured into the mixture of concentrated HCl (6 g) and ice-water (6 g). After that, the reaction mixture was stirred at rt for 30 min, additional HCl (8.8 mL, 5M) was added into the mixture, and then the reaction mixture was refluxed for 2 h. After the crude product was cooled to rt, water (100 mL) was added and the reaction mixture was extracted with DCM (2 100 mL). The combined organic layers were washed with brine and then dried (Na2SO4). After removing the solvent, the residue was purified by flash column chromatography.
With acetic anhydride; triethylamine; at 200℃; for 22h; General procedure: Phthalic anhydride (4.41 mmol) was added to a solution of Ac2O (2.4 mL) and NEt3 (1.3 mL). To the resulting orange suspension, ethyl acetoacetate (630 μL, 4.84 mmol) was quickly added. The red solution was stirred at room temperature for 22 h. Ice (1.7 g) and concentrate HCl (1.6 mL) were added followed by the addition of 5 M HCl (7 mL). The resulting mixture was stirred at 80 C for 15 min. After cooling to room temperature, the mixture was extracted with CH2Cl2. The combined organic extract was washed with brine (25 mL), dried over Na2SO4 and the solvent was removed under reduced pressure. Then, to the solution of 1H-indene-1,3(2H)-dione in 5 ml CH3CN, TsN3 (6.6 mmol) and Et3N (8 mmol) was added at 0 . The reaction mixture was allowed to warm to room temperature and stirred for 10 h. Afterwards, the reaction mixture was purified by flash column chromatography to afford the pure product 18b-18i.
 

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