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Chemical Structure| 66306-13-6 Chemical Structure| 66306-13-6

Structure of 66306-13-6

Chemical Structure| 66306-13-6

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Product Details of [ 66306-13-6 ]

CAS No. :66306-13-6
Formula : C8H9NO5S
M.W : 231.23
SMILES Code : O=C(O)C1=CC(S(=O)(NC)=O)=CC=C1O
MDL No. :MFCD11108205

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Application In Synthesis of [ 66306-13-6 ]

* 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 [ 66306-13-6 ]

[ 66306-13-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17243-13-9 ]
  • [ 74-89-5 ]
  • [ 66306-13-6 ]
YieldReaction ConditionsOperation in experiment
In ethanol; dichloromethane; at 20℃; for 1h; (b) 2-Hydroxy-5-methylsulfamoyl-benzoic acid; To 63 mmol 5-chlorosulfonyl-2-hydroxy-benzoic acid in 120 ml dichloromethane at RT was added dropwise 317 mmol methylamine (8 M solution in ethanol), and the mixture was allowed to stir at RT for 1 h. The mixture was then concentrated in vacuo. The residue was suspended in 1 M aq NaOH solution and extracted twice with ether. The aqueous phase was acidified with 5 M aq HCl, saturated with NaCl, and extracted 3 times with THF. The combined THF extracts were washed twice with saturated aqueous NaCl solution and dried with Na2SO4. Evaporation in vacuo yielded the title compound.
In ethanol; dichloromethane; at 20℃; for 1h; (b) 2-Hydroxy-5-methylsulfamoyl-benzoic acid; To 63 mmol 5-chlorosulfonyl-2-hydroxy-benzoic acid in 120 ml dichloromethane at RT was added dropwise 317 mmol methylamine (8 M solution in ethanol) and the mixture was allowed to stir at RT for 1 h. The mixture was then concentrated in vacuo. The residue was suspended in 1 M aq NaOH solution and extracted twice with ether. The aqueous phase was acidified with 5 M aq HCl, saturated with NaCl, and extracted 3 times with THF. The combined THF extracts were washed twice with saturated aqueous NaCl solution and dried with Na2SCv Evaporation in vacuo yielded the title compound. MS (m/e): 249.0 (M+NH4+, 100%), 231.9 (M+H 63%)
In dichloromethane; at 20℃; for 1h; (b) 2-Hydroxy-5-methylsulfamoyl-benzoic acid; To 63 mmol 5-chlorosulfonyl-2-hydroxy-benzoic acid in 120 ml dichloromethane at RT was added dropwise 317 mmol methylamine (8 M solution in ethanol) and the mixture was allowed to stir at RT for 1 h. The mixture was then concentrated in vacuo. The residue was suspended in 1 M aq NaOH solution and extracted twice with ether. The aqueous phase was acidified with 5 M aq HCQ, saturated with NaCl, and extracted 3 times with THF. The combined THF extracts were washed twice with saturated aqueous NaCl solution and dried with Na2SO4. Evaporation in vacuo yielded the title compound. MS (m/e): 249.0 (M+NH4+, 100%), 231.9 (M+H+, 63%)
 

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