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Chemical Structure| 7454-47-9 Chemical Structure| 7454-47-9

Structure of 7454-47-9

Chemical Structure| 7454-47-9

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Product Details of [ 7454-47-9 ]

CAS No. :7454-47-9
Formula : C12H10ClNO2S
M.W : 267.73
SMILES Code : O=S(C1=CC=C(Cl)C=C1)(NC2=CC=CC=C2)=O
MDL No. :MFCD00443139

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Application In Synthesis of [ 7454-47-9 ]

* 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 [ 7454-47-9 ]

[ 7454-47-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14752-66-0 ]
  • [ 98-95-3 ]
  • [ 7454-47-9 ]
YieldReaction ConditionsOperation in experiment
93% With sodium hydrogensulfite; In water; at 60℃; for 20h; General procedure: A mixture of sodium arylsulfinates (1.0 mmol), nitroarenes (0.5 mmol), NaHSO3 (1.0 mmol), MIL-101(Fe) (10 mg, 8 mol% of Fe) in H2O (2 mL) were stirred at 60 oC for 20 h in a sealed tube. After cooling to room temperature, the aqueous solution was extracted with ethyl acetate (3 × 3 mL), and the combined extract was dried with anhydrous Na2SO4. The solvent was removed, and the crude product was separated by a flash chromatography on a silica gel column to afford the pure product 3.
85% General procedure: In a 20 mL schlenk tube, nitrobenzene 1 (0.25 mmol), B2(OH)4 (2 mmol, 180 mg), solvent MeOH: H2O (V:V=1:1) (2 mL) were added. The reaction mixture was stirred at 100 C for 8 h. Then Ar2SO2Na 2 (0.5 mmol, 2 eq) and I2 (0.25 mmol, 1eq) were added, the mixture was stirred at 35 C for 3 h under air. After the reaction was completed, the mixture was extracted with ethyl acetate (3 × 5 mL). The combined organic layer was dried over Na2SO4 and evaporated in vacuo. The residue was purified by silica gel column chromatography to give the corresponding N-arylsulfonamides 3.
 

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