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Chemical Structure| 70415-85-9 Chemical Structure| 70415-85-9

Structure of 70415-85-9

Chemical Structure| 70415-85-9

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Product Details of [ 70415-85-9 ]

CAS No. :70415-85-9
Formula : C9H11NO2S
M.W : 197.25
SMILES Code : O=[N+](C1=CC=CC=C1SC(C)C)[O-]
MDL No. :MFCD13689000

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Application In Synthesis of [ 70415-85-9 ]

* 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 [ 70415-85-9 ]

[ 70415-85-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 70415-85-9 ]
  • [ 6397-33-7 ]
YieldReaction ConditionsOperation in experiment
96.5% With palladium 10% on activated carbon; hydrogen; In methanol; at 20℃; for 24h; 18 g (91.4mmol) 2- nitrophenyl isopropyl mercapto group intoIn a 500mL single-necked flask,Add 300mL methanol to dissolve,Then batch investment1.5 grams of 10% Pd/C,In a high purity hydrogen atmosphere,React at room temperature for 24 hours,TLC monitoring process. After the reaction,The reaction solution was filtered through celite.Concentrated and purified by silica gel column.The elution system is ethyl acetate:Petroleum ether (V/V = 1:8),Concentrated to 14.7 g of dark yellow oil.The yield was 96.5%.
1.9 kg The resulting ethyl acetate solution was added up step egret Z 400g activated carbon, 30 ~ 40 stirred for 15 to 16 hours.Removed by filtration, 2kg of ethyl acetate and washed twice.Was added to the ethyl acetate solution 140g10% Pd / C, 30 ~ 40 , 1.6atm catalytic hydrogenation, from about 19 to 20 hours to complete the reaction, the HPLC monitoring of the reaction.The catalyst was removed by filtration, and concentrated under reduced pressure to dryness to give a red oily liquid 1.9kg.
 

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