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Chemical Structure| 38131-57-6 Chemical Structure| 38131-57-6

Structure of 38131-57-6

Chemical Structure| 38131-57-6

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Product Details of [ 38131-57-6 ]

CAS No. :38131-57-6
Formula : C11H12O4S
M.W : 240.28
SMILES Code : C=C(CS(=O)(C1=CC=CC=C1)=O)C(OC)=O
MDL No. :N/A

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Application In Synthesis of [ 38131-57-6 ]

* 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 [ 38131-57-6 ]

[ 38131-57-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38131-57-6 ]
  • [ 6880-91-7 ]
  • C26H25NO6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
67% With disodium hydrogenphosphate; ruthenium(II) tris(1,10-phenanthroline) chloride hexahydrate; In N,N-dimethyl-formamide; at 20℃; for 24h;Inert atmosphere; Schlenk technique; Sealed tube; Irradiation; General procedure: As shown in Figure S1, a Schlenk tube equipped with a magnetic stir bar was charged with 0.2 mmol dihydrosanguinarine 4 (0.2 mmol), 3.0 equiv of inorganic base, 2 mol% photocatalysts, 3.0 equiv of radical Michael acceptor and 2 mL DMF under N2 atmosphere. The flask was sealed by a plastic screw-cap with a Teflon sealed inlet for a glass rod. A high power LED (λ = 455 nm) was attached to the top of the glass rod, which then could act as an optical fiber. After irradiation at room temperature for 24 h, the LED was removed, the solvent was poured to 20 mL water and extracted with 20 mL EtOAc for three times. The combined organic layer was then washed with 20 mL water for three times and evaporated giving crude product, which was purified on silica gel chromatography and eluted with PE/EtOAc to give target compounds 8.
52% With tetra-O-acetyl riboflavin; In water; acetonitrile; at 20℃; for 24h;Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; General procedure: A Schlenk tube equipped with a magnetic stir bar was charged with 0.2mmol N-phenyl tettrahydroisoquinoline, 2.0 equivalent of methyl 2-((phenylsulfonyl) methyl)acrylate, 10% of RFTA and 2 mL MeCN under N2 atmosphere. The flask was sealed by a plastic screw-cap with a Teflon sealed inlet for a glass rod. A bule light was attached to the top of the glass rod. After irradiation at room temperature for 24h, the LED was removed, the solvent was poured to 30ml water and extracted with 30mL EtOAc for three times. The organic layer was then washed with 20mL water for three times and evaporated giving crude product, which was purified on silica gel chromatography and eluted with PE/EtOAc to give target compounds.
 

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