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Chemical Structure| 106896-61-1 Chemical Structure| 106896-61-1

Structure of 106896-61-1

Chemical Structure| 106896-61-1

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Product Details of [ 106896-61-1 ]

CAS No. :106896-61-1
Formula : C12H11NO3
M.W : 217.22
SMILES Code : O=C(C1=CC2=C(C=C1)C(C(C)=O)=CN2)OC
MDL No. :MFCD16631783

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Application In Synthesis of [ 106896-61-1 ]

* 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 [ 106896-61-1 ]

[ 106896-61-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50820-65-0 ]
  • [ 75-36-5 ]
  • [ 106896-61-1 ]
YieldReaction ConditionsOperation in experiment
99% With aluminum (III) chloride; In dichloromethane; at 20℃; for 1h; To a solution of acetyl chloride (0.23 mL, 3.3 mmole) and aluminum chloride (0.88 g, 6.6 mmol) in methylene chloride (30 mL) was added l//-<strong>[50820-65-0]indole-6-carboxylic acid methyl ester</strong> (0.53 g, 3.0 mmol). After stirring 1 hr at room temperature water (300 mL) was added and then this was extracted with ethyl acetate (300 mL). The organic layer was dried (MgSO4), filtered and concentrated to collect 0.65 g (99% yield) of 3-acetyl-l/f-indole-6- carboxylic acid methyl ester a light yellow solid. 1H NMR (300 MHz, DMSO) δ 12.27 (s, IH), 8.52 (s, IH), 8.24 (d, IH, J= 8.2 Hz), 8.08 (d, IH, J= 1.0 Hz), 7.78 (dd, IH, J= 8.2, 1.0 Hz), 3.86 (s, 3H), 2.47 (s, 3H).
625 mg With aluminum (III) chloride; In dichloromethane; at 20℃; for 1h; To a solution of <strong>[50820-65-0]methyl indole-6-carboxylate</strong> (1.01 g) in dichloromethane (30 mL) were added aluminum chloride (1.53 g) and acetyl chloride (0.5 mL) at room temperature, and then the reaction mixture was stirred at room temperature for 1 hour. To the reaction mixture was added a saturated aqueous solution of sodium hydrogen carbonate, and extracted with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the titled compound (625 mg) as a white solid. 1H-NMR (400 MHz, CD3OD) δ: 8.34 (1H, s), 8.29 (1H, dd, J = 8.5, 0.7 Hz), 8.15 (1H, dd, J = 1.5, 0.7 Hz), 7.87 (1H, dd, J = 8.5, 1.5 Hz), 3.92 (3H, s), 2.54 (3H, s).
 

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