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Chemical Structure| 19446-96-9 Chemical Structure| 19446-96-9

Structure of 19446-96-9

Chemical Structure| 19446-96-9

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Product Details of [ 19446-96-9 ]

CAS No. :19446-96-9
Formula : C9H8O3S
M.W : 196.22
SMILES Code : O=S1(CCC(C2=CC=CC=C21)=O)=O
MDL No. :MFCD00461296

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Application In Synthesis of [ 19446-96-9 ]

* 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 [ 19446-96-9 ]

[ 19446-96-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3528-17-4 ]
  • [ 19446-96-9 ]
YieldReaction ConditionsOperation in experiment
80% With sodium hydrogen sulphite; sodium carbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; Example 1 Synthesis of 3,4-dihydro-2H-1-benzothiopyran-4-one 1,1-dioxide (Compound 1) 12.94 g (60 mmol) of 80% m-chloroperbenzoic acid was added in portions to a solution of 3.28 g (20 mmol) of thiochroman-4-one in methylene chloride (250 ml) while stirring under cooling with ice. The mixture was stirred at 0 C. for one hour and then at room temperature for 43 hours. The reaction mixture was filtered, and the filtrate was washed with a 10% aqueous solution of sodium carbonate, 20% aqueous solution of sodium hydrogen sulfite (twice), 10% aqueous solution of sodium carbonate (twice), and saturated brine, dried over anhydrous sodium sulfate, and concentrated under vacuum. The resultant crude product was recrystallized from ethanol to obtain 3.14 g (yield: 80%) of the title compound.
70% With dihydrogen peroxide; acetic acid; In water; at 100℃; for 1h; 1,1-Dioxo-1-thiochroman-4-one. Into a round bottom flask containing thiochroman-4-one (0.804 g, 4.75 mmol), 6 mL of glacial HOAc and, 2.3 mL of a 35% w/w solution of H2O2 (0.914 g, 26.9 mmol) were added and, the solution was heated at 100 C. for 1 h. After the reaction mixture was cooled at room temperature, 10 mL of H2O were added and the product was extracted twice with CH2Cl2 from the aqueous layer. The resultant organic phase was washed once with brine and dried under Na2SO4. After the solvent was removed, a solid was formed which was purified by recrystallization with EtOH. After drying the solid under reduced pressure, 0.649 g (3.31 mmol) of the product was obtained in a 70% yield. 1H NMR (300 MHz, acetone-d6, δ): 8.07 (ddd, J=7.7, 1.3, 0.6, Ar, 1H), 7.99 (ddd, J=7.8, 2.2, 0.7, Ar, 1H), 7.95 (td, J=7.8, 1.5, Ar, 1H), 7.86 (ddd, J=7.7, 6.7, 2.1, Ar, 1H), 3.94 (t, J=6.3, C2, 2H), 3.37 (t, J=6.3, C2, 2H). 13C NMR (75 MHz, acetone-d6): δ 191.3, 142.9, 135.6, 134.1, 131.6, 129.1, 124.0, 49.6, 37.5. Dept 45 NMR (75 MHz, acetone-d6): δ 134.8 (H), 133.2 (H), 128.2 (H), 123.1 (H), 48.8 (H2), 36.7 (H2).
 

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