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Chemical Structure| 879093-03-5 Chemical Structure| 879093-03-5

Structure of 879093-03-5

Chemical Structure| 879093-03-5

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Product Details of [ 879093-03-5 ]

CAS No. :879093-03-5
Formula : C9H7ClF2O2
M.W : 220.60
SMILES Code : O=C(OCC)C1=CC(F)=C(Cl)C=C1F
MDL No. :MFCD12025299

Safety of [ 879093-03-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 879093-03-5 ]

* 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 [ 879093-03-5 ]

[ 879093-03-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 132794-07-1 ]
  • [ 64-17-5 ]
  • [ 879093-03-5 ]
YieldReaction ConditionsOperation in experiment
94% sulfuric acid; for 18h;Heating / reflux; Sulfuric acid (62.4 ml, 1.13 moles) was added to a solution of <strong>[132794-07-1]2,5-difluoro-4-chloro-benzoic acid</strong> (750.0 g, 3.895 moles) (PLEASE DEFINE THE SOURCE OF THIS REACTANT) in absolute ethanol (3.75 L). The mixture was refluxed for 18 hours. The mixture was concentrated to remove most of ethanol and then cooled to room temperature. The residue was neutralized with 1N aqueous NaOH (2.4 L) and extracted with ethyl acetate (2×1L). The combined extracts were washed with sat. aqueous NaHCO3 and brine, then dried with (MgSO4) and concentrated to dryness. Ethyl 2,5-difluoro-4-chloro-benzoate (806.7 g) was obtained at 94% yield. 1H NMR (in CDCl3): delta7.72 (dd, J=9.1/6.2, 1H), 7.22 (dd, J=9.1/5.6, 1H), 4.39 (q, 3J=7.0, 2H), 1.39 (t, J=7.0, 3H). GC-MS: 161 (M+).
With sulfuric acid; for 72h;Heating / reflux; Preparation 1 4-Chloro-2,5-difluoro-benzaldehyde <strong>[132794-07-1]4-Chloro-2,5-difluoro-benzoic acid</strong> (25.0 g, 129.84 mmol), H2SO4 (3.46 mL, 64.92 mmol) and EtOH (300 mL) were combined and heated at reflux for 72 h. The solution was cooled, concentrated, diluted with H2O (1.0 L), and extracted with EtOAc (3*500 mL). The combined organic extracts were washed with saturated NaHCO3 (3*200 mL), H2O (200 mL), dried (MgSO4), filtered, and concentrated to provide 28.17 g of <strong>[132794-07-1]4-chloro-2,5-difluoro-benzoic acid</strong> ethyl ester as a golden oil.
 

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