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Chemical Structure| 20240-61-3 Chemical Structure| 20240-61-3

Structure of 20240-61-3

Chemical Structure| 20240-61-3

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Product Details of [ 20240-61-3 ]

CAS No. :20240-61-3
Formula : C11H14O
M.W : 162.23
SMILES Code : OC1CCC(C)C2=C1C=CC=C2
MDL No. :MFCD24205505

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Application In Synthesis of [ 20240-61-3 ]

* 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 [ 20240-61-3 ]

[ 20240-61-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 19832-98-5 ]
  • [ 20240-61-3 ]
YieldReaction ConditionsOperation in experiment
To a stirred solution of commercially available 4-methyl-alpha-tetralone (0.50 g, 3.12 mmol) in methanol (50 mL) was added NaBH4 (0.35 g, 9.36 mmol) portionwise. The reaction mixture was followed by TLC and, after complete consumption of the starting material (approx. 2 h), was quenched with saturated NaHCO3. The aqueous layer was extracted with diethyl ether, dried with magnesium sulfate (MgSO4), filtered, and the solvent was removed under reduced pressure. The crude alcohol was dissolved in toluene (15 mL), and a few crystals of p-TsOH were added. The reaction mixture was stirred overnight, then neutralized by slow addition of saturated sodium bicarbonate (NaHCO3) and extracted with diethyl ether. The combined organic layers where washed with brine, dried with magnesium sulfate (MgSO4), filtered, and the solvent was removed under reduced pressure. The product was purified by flash chromatography (SiO2, hexanes) to give 1,2-dihydro-1-methylnaphthalene ((+/-)-8) as a clear oil (0.35 g, 78% yield). The compound is volatile and cannot be dried for long periods (>30 min) under high vacuum. The spectroscopic data are consistent with previously reported data (Ferraz, which is hereby incorporated by reference).
  • 2
  • [ 19832-98-5 ]
  • [ 20240-61-3 ]
  • 3
  • [ 19832-98-5 ]
  • [ 20240-61-3 ]
 

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