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Chemical Structure| 2728-74-7 Chemical Structure| 2728-74-7

Structure of 2728-74-7

Chemical Structure| 2728-74-7

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Product Details of [ 2728-74-7 ]

CAS No. :2728-74-7
Formula : C7H4ClFO2
M.W : 174.56
SMILES Code : O=C(Cl)C1=CC(F)=CC=C1O

Safety of [ 2728-74-7 ]

Application In Synthesis of [ 2728-74-7 ]

* 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 [ 2728-74-7 ]

[ 2728-74-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64628-73-5 ]
  • [ 2728-74-7 ]
  • C14H8ClF4NO3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 25℃;Inert atmosphere; General procedure: A dry, 50 mL round bottom flask was charged with a magnetic stir bar then sealed with a septum and flushed with nitrogen. To this was added the salicylic acid derivative (2.0 mmol) and dichloromethane (10 mL). While stirring, SOCl2 (10 mmol) was added dropwise, followed by dimethylformamide (0.05 mmol), and the mixture was allowed to stir at room temperature under nitrogen for 12 hours. At this point, the mixture was concentrated under vacuum to afford the solid acid chloride derivative which was used immediately without further purification. The flask containing the acid chloride was then re-sealed with a septum and placed under a nitrogen atmosphere, and its contents were re-suspended in fresh dichloromethane (20 mL). While stirring, the aniline derivative (4.0 mmol) was added and the resulting opaque mixture was stirred for an additional 18 h. At this point, the mixture was quenched with ice water (5 mL) and phases were separated using a separatory funnel. The aqueous layer was extracted twice with dichloromethane (20 mL) then the organic layers were combined and washed with brine (40 mL). The organic layer was then dried over Na2SO4, filtered, and concentrated under vacuum to afford a crude solid residue. This residue was then re-suspended in dichloromethane (10 mL) and adsorbed onto silica gel (1 g), then chromatographed on a 12 g silica gel column using a solvent gradient of 0-40% ethyl acetate in hexanes over 25 min. The product-containing fractions were combined then concentrated under vacuum to afford the purified salicylamide derivative.
 

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