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Chemical Structure| 491-39-4 Chemical Structure| 491-39-4

Structure of 491-39-4

Chemical Structure| 491-39-4

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Product Details of [ 491-39-4 ]

CAS No. :491-39-4
Formula : C9H6OS
M.W : 162.21
SMILES Code : O=C1C=CSC2=CC=CC=C12
MDL No. :MFCD00094950

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Application In Synthesis of [ 491-39-4 ]

* 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 [ 491-39-4 ]

[ 491-39-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3528-17-4 ]
  • [ 491-39-4 ]
YieldReaction ConditionsOperation in experiment
With N-chloro-succinimide; In dichloromethane; at 20℃; for 12h;Cooling with ice; General procedure: To a cool solution (ice bath) of C (10 mmol) in CH2Cl2 (30 ml) was added N-chlorosuccinimide (NCS) (10.5mmol, 1.05 equivalent) in one portion. The resultant mixture was then warmed up to room temperatureand stirred overnight for about 12 hours. It was quenched with water (30 ml) and the organic layer wasseparated. The aqueous layer was extracted with DCM (2 X 30 mL). The organic layers were combinedand dried (Na2SO4). It was then filtered, concentrated under vacuum to give crude product. The crudeproduct was then purified by flash column chromatography (EtOAc/hexanes, 5-10%) to givethiochromone D in 50-70% yield.
With N-chloro-succinimide; In dichloromethane; at 0 - 20℃; General procedure: To a solution of S3 (30.5 mmol) in CH2Cl2 (100 ml) was added N-chlorosuccinimide(NCS) (30.5 mmol, 1.0 equive) in one portion. This was stirred for 20 min at 0 oC,and then allowed to warm to room temprature overnight. Water (50 ml) was addedand the organic layer was separated and dried (Na2SO4), and the product purified bycolumn chromatography (hexane/ acetone, 5/1) to give thiochromone S4 in 40-80%yield.
 

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