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[ CAS No. 59724-53-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 59724-53-7
Chemical Structure| 59724-53-7
Structure of 59724-53-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 59724-53-7 ]

CAS No. :59724-53-7 MDL No. :MFCD02225949
Formula : C10H15NO3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 229.30 Pubchem ID :-
Synonyms :

Safety of [ 59724-53-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 59724-53-7 ]

* 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 [ 59724-53-7 ]

[ 59724-53-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 384-64-5 ]
  • [ 59724-53-7 ]
  • C19H20FNO3S [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With lithium hydroxide In dimethyl sulfoxide at 40℃; for 12h; Schlenk technique; chemoselective reaction; 2.1 Procedure for defluorinative cyclization of (trifluoromethyl)alkenes with amino alcohols General procedure: In a 25 mL oven-dried Schlenk tube equipped with a magneticstirring bar, amino alcohols 1 (0.2 mmol), (trifluoromethyl)-alkenes 2 (0.4 mmol), t-BuOLi or LiOH(0.8 mmol), and dimethyl sulfoxide (DMSO, 2 mL) werevigorously stirred at 40 °C for 12 h. Then the stirring wasstopped. Add water (15 mL) to the mixture, which wassuccessively extracted with EtOAc (15 mL×3). The combinedorganic phases were dried over anhydrous Na2SO4,filtered and concentrated in vacuo. Further purification byflash column chromatography on silica gel (eluting with petroleum ether/ethyl acetate) provided the product 3 or 4.
  • 2
  • [ 69843-10-3 ]
  • [ 59724-53-7 ]
  • C19H19ClFNO3S [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% With lithium hydroxide In dimethyl sulfoxide at 40℃; for 12h; Schlenk technique; chemoselective reaction; 2.1 Procedure for defluorinative cyclization of (trifluoromethyl)alkenes with amino alcohols General procedure: In a 25 mL oven-dried Schlenk tube equipped with a magneticstirring bar, amino alcohols 1 (0.2 mmol), (trifluoromethyl)-alkenes 2 (0.4 mmol), t-BuOLi or LiOH(0.8 mmol), and dimethyl sulfoxide (DMSO, 2 mL) werevigorously stirred at 40 °C for 12 h. Then the stirring wasstopped. Add water (15 mL) to the mixture, which wassuccessively extracted with EtOAc (15 mL×3). The combinedorganic phases were dried over anhydrous Na2SO4,filtered and concentrated in vacuo. Further purification byflash column chromatography on silica gel (eluting with petroleum ether/ethyl acetate) provided the product 3 or 4.
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