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Chemical Structure| 191602-86-5 Chemical Structure| 191602-86-5

Structure of 191602-86-5

Chemical Structure| 191602-86-5

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Product Details of [ 191602-86-5 ]

CAS No. :191602-86-5
Formula : C13H10BrNO3
M.W : 308.13
SMILES Code : O=[N+](C1=CC=C(OCC2=CC=CC=C2)C(Br)=C1)[O-]
MDL No. :MFCD18447619

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Application In Synthesis of [ 191602-86-5 ]

* 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 [ 191602-86-5 ]

[ 191602-86-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5847-59-6 ]
  • [ 100-39-0 ]
  • [ 191602-86-5 ]
YieldReaction ConditionsOperation in experiment
79% With potassium carbonate; In acetone; at 60℃; for 12h; Benzyl bromide (83 mL, 0.702 mmol) was added drop-wise to a solution of 2-bromo-4- nitrophenol (170 g, 0.780 mmol) and potassium carbonate (323 g, 2.34 mmol) in acetone (1 L) and refluxed at 60 C for 12 h. The reaction mixture was filtered through celite and washed with 200 mL ethyl acetate. The solvent was removed, triturated withhexane (400 mL) at 60 C to obtain the title compound.Yield: 190 g (79 %); 1H NMR (300 MHz, DMSO-d6): O 5.37 (5, 2H, CH2), 7.33-7.50 (m, 6H, Ar), 8.27 (dd, J = 2.4 Hz, 9.1 Hz, 1H, Ar), 8.45 (d, J = 2.4 Hz, 1H, Ar).
With potassium carbonate; In acetone; for 5h;Reflux; 4-Nitrophenol (5.00g, 35.9mmol) was dissolved in concentrated sulfuric acid (40ml) at room temperature. The solution was cooled to 0C, and N-bromosuccinimide (6.40g, 36.0mmol) was added portionally. Once the complete conversion was detected, the mixture was poured onto ice. The resulted precipitates were collected by filtration, washed with water, and dried. The above-obtained crude <strong>[5847-59-6]2-bromo-4-nitrophenol</strong> was dissolved in acetone (100ml), and stirred with potassium carbonate (12.5g, 90.4mmol) and benzyl bromide (6.20g, 36.2mmol) under reflux for 5h. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by flash column chromatography (petroleum ether/ethyl acetate 20:1-9:1) to give the title compound as a light yellow solid (8.38g, 76% for two steps).
With potassium carbonate; In acetone; at 70℃; for 20h;Sealed tube; General procedure: (iii) A mixture of 3-bromo-4-nitro-1-naphthanol (1mmol), BnBr (3 mmol, 0.35 mL), and K2CO3 (2 mmol) inacetone (3 mL) was heated to 70oC for 20 h in a sealed tube.The mixture was diluted with ethyl acetate (20 mL), washedwith water (2 x 10 mL), dried over anhydrous Na2SO4 andconcentrated. Hexane (1 mL) was added into the resulting residue to give benzyl protected 3-bromo-4-nitro-1-naphthanol as a yellow solid 5 in ~90% yield.
 

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