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Chemical Structure| 4830-94-8 Chemical Structure| 4830-94-8

Structure of 4830-94-8

Chemical Structure| 4830-94-8

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Product Details of [ 4830-94-8 ]

CAS No. :4830-94-8
Formula : C10H13Cl
M.W : 168.66
SMILES Code : CC(Cl)CCC1=CC=CC=C1

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Application In Synthesis of [ 4830-94-8 ]

* 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 [ 4830-94-8 ]

[ 4830-94-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4830-94-8 ]
  • [ 100-58-3 ]
  • [ 1520-44-1 ]
YieldReaction ConditionsOperation in experiment
74% With copper(l) iodide; In 2-methyltetrahydrofuran; toluene; at 80℃; for 18.0h;Inert atmosphere; Schlenk technique; Sealed tube; General procedure: To an oven-dried Schlenk tube were added CuI (0.1 mmol, 10 mol%), then the tube was evacuated and backfilled with argon for three times. To this Schlenk tube were added alkyl chloride (1.0 mmol), toluene (2.0 mL) and phenylmagnesium bromide (0.8 mL of a 2.9 mol/L 2-MeTHF solution, 2.3 mmol). The tube was sealed and the mixture was allowed to stir at 80 C for 18 h. After being cooled to room temperature, the reaction mixture was quenched with HCl aq. (1 N). The aqueous layer was extracted with Et2O three times. The combined organic layer was dried over anhydrous MgSO4, filtered, and evaporated. The residue was purified by column chromatography using petroleum ether (30 - 60oC) as eluent to afford the product.
74% With copper(l) iodide; In 2-methyltetrahydrofuran; toluene; at 80℃; for 12.0h;Schlenk technique; Inert atmosphere; To the Schlenk reaction tube, 19 mg (0.1 mmol) of cuprous iodide was added, and a vacuum was applied using a Schlenk double-row tube, and argon gas was introduced thereto, and it was repeated three times.Under argon, add 168 uL (1.0 mmol) of 1-phenyl-3-chlorobutane, 2.0 mL of toluene, 2.4 mL of phenylmagnesium bromide (2.4 mmol, 1.0 mol/L, 2-methyltetrahydrofuran solution).),The reaction system was sealed, and the reaction tube was placed in an 80 C oil bath. After stirring for 12 hours, 3 mL of dilute hydrochloric acid (concentration 1 mol/L) and 10 mL of petroleum ether (boiling range 30-60 C) were added.After stirring for 10 minutes, the extract was separated, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated and then purified by silica gel column chromatography, eluent petroleum ether (boiling range 30 to 60 C), yield 74%.
 

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