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Chemical Structure| 573-99-9 Chemical Structure| 573-99-9

Structure of 573-99-9

Chemical Structure| 573-99-9

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Product Details of [ 573-99-9 ]

CAS No. :573-99-9
Formula : C11H9F
M.W : 160.19
SMILES Code : CC1=CC=C2C=CC=CC2=C1F
English Name :1-Fluoro-2-methylnaphthalene
MDL No. :MFCD09029697

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* 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 [ 573-99-9 ]

[ 573-99-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2246-44-8 ]
  • [ 573-99-9 ]
YieldReaction ConditionsOperation in experiment
67% Stage #1: 1-amino-2-methylnaphthalene With tetrafluoroboric acid; sodium nitrite for 0.5h; Cooling with ice; Stage #2: In toluene at 90℃; for 3h; 49 Add 2-methyl-1-naphthylamine (1.57 g, 10 mmol) to a 100 mL eggplant-shaped bottle,Fluoroboric acid (15 mL) was added dropwise to the reaction flask, and cooled in an ice bath.Slowly add 10 mL of NaNO2 solution (2.76 g, 40 mmol) to the reaction solution,Reaction in an ice bath for 0.5 h, suction filtration, and the filter cake was dried to obtain diazonium salt.The obtained diazonium salt was added to 50 mL of toluene, and the reaction was carried out at 90 ° C. for 1 h and refluxed for 2 h.The reaction solution was washed with a saturated NaHCO3 solution and a saturated saline solution in this order,After drying over anhydrous sodium sulfate, the reaction solution was concentrated and purified through a column to obtain 1-fluoro-2-methylnaphthalene with a yield of 67%.
(i) (diazotization), (ii) HPF6, (iii) (pyrolysis); Multistep reaction;
Multi-step reaction with 2 steps 1: nitrite source / Acidic conditions; Cooling 2: lithium tetrafluoroborate / Hexafluorobenzene; ethyl acetate / 2 h / 90 °C / Sealed tube
 

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