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Chemical Structure| 25245-33-4 Chemical Structure| 25245-33-4

Structure of 25245-33-4

Chemical Structure| 25245-33-4

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Product Details of [ 25245-33-4 ]

CAS No. :25245-33-4
Formula : C8H9IO2
M.W : 264.06
SMILES Code : COC1=CC=CC(I)=C1OC
MDL No. :MFCD05864318

Safety of [ 25245-33-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 25245-33-4 ]

* 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 [ 25245-33-4 ]

[ 25245-33-4 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 25245-33-4 ]
  • [ 19337-60-1 ]
YieldReaction ConditionsOperation in experiment
22% With boron tribromide; In dichloromethane; at 0 - 20℃; for 3.0h; 1-Iodo-2,3-dimethoxybenzene (0.62 g, 2.35 mmol) obtained in Step A was dissolved in DCM (23 mL) andcooled to 0-5°C. 1M BBr3 (0.276 mL, 7.05 mmol) was slowly added thereto, and the mixture was stirred at room temperaturefor 3 hours. After termination of the reaction, the reaction solution was cooled to -20°C and diluted by slowlyadding ethanol. The mixure was stirred at room temperature for 30 minutes, and saturated NaHCO3 aqueous solutionwas added thereto. The mixture was extracted with DCM. The organic layer was dried with MgSO4, concentrated underreduced pressure and purified by column chromatography (eluent, EtOAc/Hex = 1/4) to obtain the title compound (0.12g, 22 percent).1H NMR (500 MHz, CDCl3) delta 7.18(d, 1H), 6.87(d, 1H), 6.60(t, 1H), 5.64(s, br, 2H)
To a stirred solution of 1-iodo-2,3-bis(methyloxy)benzene (1.01 g) in dry DCM (6 ml.) under nitrogen at -450C was added a solution of boron tribromide (1M in DCM, 4.24 ml_). After 0.5 h at -450C the cooling bath was removed and the mixture was allowed to stir at room temperature for 1 h. The mixture was then cooled to -90C and water was added dropwise with stirring. The organics were separated using a hydrophobic frit and the aqueous phase was extracted with DCM. The combined organics were evaporated in vacuo to give the title compound. MS calcd for (C6H5IO2 - H)": 235 MS found (electrospray): (M-H)" = 235
 

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