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Chemical Structure| 117113-98-1 Chemical Structure| 117113-98-1

Structure of 117113-98-1

Chemical Structure| 117113-98-1

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Product Details of [ 117113-98-1 ]

CAS No. :117113-98-1
Formula : C14H13FO2
M.W : 232.25
SMILES Code : FC1=CC=C(C=C1)COC2=CC=C(C=C2)CO
MDL No. :MFCD00173648

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Application In Synthesis of [ 117113-98-1 ]

* 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 [ 117113-98-1 ]

[ 117113-98-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56442-17-2 ]
  • [ 117113-98-1 ]
YieldReaction ConditionsOperation in experiment
95% With sodium tetrahydroborate; In methanol; at 20℃; for 3h; General procedure: Sodium borohydride (5.4 mmol) was added portion-wise to the solution of compound 3 (5.4 mmol) in methanol (40 ml) and the mixture was stirred at room temperature for 3 h. After evaporation of methanol, the resulting residue was neutralized with a solution of hydrochloric acid (1 M) to pH 6-8. The mixture was extracted with dichloromethane. The organic layer was dried over anhydrous Na2SO4, concentrated to produce the white solid.
With sodium tetrahydroborate; In tetrahydrofuran; ethanol; at 0℃; for 12h;Inert atmosphere; General procedure: A 100mL oven-dried three-neck flask was charged with magnetic bead, 20mmol of 6 (6a-6f), flushed with dry nitrogen gas followed by addition of ethanol (40mL), dry THF (20mL), and NaBH4 (1.14g, 30mmol) under inert conditions at 0C. The mixture was then stirred for 12h. When TLC analysis confirmed that the reaction was completed, 2N HCl was drop-wise added to decompose excess NaBH4 while stirring was continued. The solution was evaporated and the residue was extracted with dichloromethane followed by its washing with water. Combined organic phases were dried over Na2SO4 and concentrated to give desired product 7 (7a-7f) in 93%-96% yields.
 

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