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Chemical Structure| 863870-77-3 Chemical Structure| 863870-77-3

Structure of 863870-77-3

Chemical Structure| 863870-77-3

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Product Details of [ 863870-77-3 ]

CAS No. :863870-77-3
Formula : C11H13ClINO2
M.W : 353.58
SMILES Code : O=C(OC1=CC=CC(Cl)=C1I)N(CC)CC
MDL No. :MFCD08166411

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Application In Synthesis of [ 863870-77-3 ]

* 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 [ 863870-77-3 ]

[ 863870-77-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 863870-77-3 ]
  • [ 858854-82-7 ]
YieldReaction ConditionsOperation in experiment
100% With ethanol; sodium hydroxide; at 25℃; for 2h;Inert atmosphere; Reflux; (c) Step 3 Sodium hydroxide (32.0 g, 800 mmol) was added at 25 C. to 400 mL of an ethanol solution of 3-chloro-2-iodophenyl N,N-diethylcarbamate (57.0 g, 161 mmol), and the reaction solution was heated and refluxed for two hours. The ethanol was distilled off under reduced pressure, and the residue was dissolved in 400 mL of water and extracted by petroleum ether. The water layer was neutralized by 2N hydrochloric acid, and extracted by ethyl acetate. The combined organic layers were washed with (saturated) brine, dried with anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 3-chloro-2-iodophenol (41.0 g, quantitative). 1H NMR (400 MHz, CDCl3) delta 5.58 (brs, 1H), 6.90 (dd, J=1.2, 8.4 Hz, 1H), 7.06 (dd, J=1.2, 8.0 Hz, 1H), 7.21 (t, J=8.0 Hz, 1H).
Carbamate 185 (10 g, 28 mmol, 1 eq) was treated with sodium hydroxide (11 g, 283 mmol, 10 eq) in refluxing ethanol (140 mL). After 14 h, the solution was allowed to cool to rt, acidified with HCl 6N then extracted with DCM (3×60 mL). The combined organics were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (Hexane/DCM 0% to 100%) to obtain 186 an oil (3.75 g, 15 mmol). Yield 52%.
 

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