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Chemical Structure| 3558-06-3 Chemical Structure| 3558-06-3

Structure of 3558-06-3

Chemical Structure| 3558-06-3

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Product Details of [ 3558-06-3 ]

CAS No. :3558-06-3
Formula : C12H16O3S
M.W : 240.32
SMILES Code : O=S(C1=CC=C(C)C=C1)(OC2CCCC2)=O

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Application In Synthesis of [ 3558-06-3 ]

* 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 [ 3558-06-3 ]

[ 3558-06-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3558-06-3 ]
  • [ 84478-72-8 ]
  • [ 141772-32-9 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; potassium iodide; tetrabutylammomium bromide; In water; toluene; STR120 A solution of <strong>[84478-72-8]2-chloro-4-fluoro-5-aminophenol</strong> (1.02 g, 6.29 mmol), cyclopentyl p-toluenesulfonate (1.56 g, 6.50 mmol), tetrabutylammonium bromide (242 mg, 0.75 mmol) and potassium iodide (262 mg, 1.57 mmol) in toluene (20 ml) was prepared in a 50 cc three-necked round bottom flask equipped with a stirrer. Then, a 40% aqueous sodium hydroxide solution (20 ml) was added slowly thereto, followed by stirring while heating at 100 C. for 2 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water (10 ml) was added thereto, and the mixture was extracted with ethyl acetate (20 ml*3 portions). The organic layers were combined, washed with water (10 ml) and a saturated aqueous sodium chloride solution (10 ml) and dried over anhydrous magnesium sulfate. After removing the drying agent, the solvent was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5-cyclopentyloxyaniline (1.44 g, 6.27 mmol, 99.6% yield).
With sodium hydroxide; potassium iodide; tetrabutylammomium bromide; In water; toluene; EXAMPLE 5 STR12 A round-bottomed flask (50 cc) equipped with a mechanical stirrer was charged with <strong>[84478-72-8]5-amino-2-chloro-4-fluorophenol</strong> (1.02 g, 6.29 mmol), cyclopentyl p-toluenesulfonate (1.56 g, 6.50 mmol), tetrabutylammonium bromide (242 mg, 0.75 mmol) and potassium iodide (262 mg, 1.57 mmol) to prepare a solution in toluene (20 mL). Subsequently, 40% sodium hydroxide in aqueous solution (20 mL) was added slowly and the mixture was stirred under heating at 100 C. for 2 h. After completion of the reaction, the reaction mixture was cooled to room temperature and water (10 mL) was added, followed by extraction with ethyl acetate (20 mL*3). The organic layers were combined, washed with water (10 mL) and saturated brine (10 mL) and dried with anhydrous magnesium sulfate. After the desiccant was removed, the solvent was distilled off under vacuum to give 4-chloro-5-cyclopentyloxy-2-fluoroaniline (1.44 g, 6.27 mmol; yield=99.6%).
 

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