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Chemical Structure| 2510-49-8 Chemical Structure| 2510-49-8

Structure of 2510-49-8

Chemical Structure| 2510-49-8

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Product Details of [ 2510-49-8 ]

CAS No. :2510-49-8
Formula : C9H11IO3
M.W : 294.09
SMILES Code : COC1=CC(OC)=C(I)C(OC)=C1
MDL No. :MFCD00598379

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Application In Synthesis of [ 2510-49-8 ]

* 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 [ 2510-49-8 ]

[ 2510-49-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 570-02-5 ]
  • [ 2510-49-8 ]
YieldReaction ConditionsOperation in experiment
95% With N-iodo-succinimide; palladium diacetate; In N,N-dimethyl-formamide; at 80℃; for 3h;Inert atmosphere; Sealed tube; A mixture of <strong>[570-02-5]2,4,6-trimethoxybenzoic acid</strong> (42.4 mg, 0.2 mmol), NIS (47.3 mg, 0.21 mmol)Palladium acetate (0.9 mg, 0.002 mmol), and a stirrer were placed in the reaction tube and replacedAfter the inert gas was added, 1 ml of solvent DMF was added and sealedReaction tube. The reaction tube was placed in an oil bath reaction reactor at 80 C and stirred for 3 hours. After cooling to room temperature, use 2 mol / L of hydrogen Sodium oxide solution to adjust pH = 10. The reaction tube was diluted with 5 ml of water and extracted with ethyl acetate. Merge the extract and Dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and washed with ethyl acetate: petroleum ether = 0 to 1: 30 (volume ratio) The crude product was subjected to column chromatography to give pure 2,4,6-trimethoxyiodobenzene (55.9 mg, 95%).
79% With oxygen; copper (I) acetate; silver sulfate; sodium iodide; In dimethyl sulfoxide; at 160℃; for 24h;Schlenk technique; Silak reaction tube equipped with a magnetic stirrer was charged with 3.1 mg of silver sulfate,36.3 mg of copper acetate, 42.4 mg of <strong>[570-02-5]2,4,6-trimethoxybenzoic acid</strong>,149.9 mg of sodium iodide and 1 mL of dimethylsulfoxide.The reaction was heated at 160 C for 24 hours in the presence of oxygen.After the reaction was completed, distilled water was added to quench the reaction,Extraction with ethyl acetate 3 times, each time 10mL,The combined organic phases were concentrated to give 46.5 mg of 2,4,6-trimethoxy-iodobenzene,The yield is 79%.
  • 2
  • [ 570-02-5 ]
  • [ 2510-49-8 ]
  • [ 117934-81-3 ]
 

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