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Chemical Structure| 4514-28-7 Chemical Structure| 4514-28-7

Structure of 4514-28-7

Chemical Structure| 4514-28-7

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Product Details of [ 4514-28-7 ]

CAS No. :4514-28-7
Formula : C13H10BrNO3
M.W : 308.13
SMILES Code : O=[N+](C1=CC(OCC2=CC=CC=C2)=CC=C1Br)[O-]
MDL No. :MFCD28098598

Safety of [ 4514-28-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 4514-28-7 ]

* 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 [ 4514-28-7 ]

[ 4514-28-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 78137-76-5 ]
  • [ 100-44-7 ]
  • [ 4514-28-7 ]
  • 2
  • [ 78137-76-5 ]
  • [ 100-39-0 ]
  • [ 4514-28-7 ]
YieldReaction ConditionsOperation in experiment
78% With potassium carbonate; In acetone; acetonitrile; for 17h;Heating / reflux; Benzyl bromide (131 mmol) and potassium carbonate (130 mmol) were added to a solution of the nitrophenol (87.0 mmol) in 2/1 acetonitrile/acetone (840 mL). The reaction mixture was heated at reflux for 17 h and was concentrated to dryness. The residue was suspended in ethyl acetate (756 mL), filtered, and the organic layer was washed with water (567 mL), 1 M hydrochloric acid (2*567 mL), and brine (567 mL). The organic layer was dried (magnesium sulfate) and concentrated to the benzyl ether in 78percent yield.
78% With potassium carbonate; In acetone; acetonitrile; for 17h;Heating / reflux; Benzyl bromide (131 mmol) and potassium carbonate (130 mmol) were added to a solution of the nitrophenol (87.0 mmol) in 2/1 acetonitrile/acetone (840 mL). The reaction mixture was heated at reflux for 17 h and was concentrated to dryness. The residue was suspended in ethyl acetate (756 mL), filtered, and the organic layer was washed with water (567 mL), 1 M hydrochloric acid (2 x 567 mL), and brine (567 mL). The organic layer was dried (magnesium sulfate) and concentrated to the benzyl ether in 78percent yield.
With potassium carbonate; In water; acetone; A. Preparation of 5-benzyloxy-2-bromonitrobenzene <strong>[78137-76-5]2-Bromo-5-hydroxynitrobenzene</strong> (1.0 g) was dissolved in acetone (50 mL). Potassium carbonate (3.5 g) and benzyl bromide (1.2 mL) were added, and the resulting mixture was stirred at room temperature for 3 hours. After the reaction was completed, water (100 mL) was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried. The solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (19:1 hexane/ethyl acetate) to yield the title compound (1.42 g). Rf=0.38 (9:1 hexane/ethyl acetate); 1H-NMR (DMSO-d6): 7.79 (1H, d, J=9.1), 7.74 (1H, d, J=3.0), 7.35-7.48 (5H, m), 7.28 (1H, dd, J=9.1, 3.0), 5.20 (2H, s); Mass (m/e): 309 (MH+).
8.7 g (100%) With potassium carbonate; In N-methyl-acetamide; A. 2-Bromo-5-benzyloxy-nitrobenzene To a solution of 6.2 g (28.4 mmol) of <strong>[78137-76-5]4-bromo-3-nitrophenol</strong> in 30 mL of dimethylformamide, 5.35 g (31.3 mmol) of benzyl bromide and 4.32 g (31.3 mmol) of potassium carbonate were added and the mixture was stirred at room temperature overnight. The mixture was poured into 300 mL of ice/water and extracted with ethyl acetate (3*150 mL) and the combined organic solutions were dried and evaporated to provide 8.7 g (100percent) of compound A as a straw-colored oil.
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 3h; To a mixture of <strong>[78137-76-5]4-bromo-3-nitrophenol</strong> (5 g, 22.94 mmol, 1.00 equiv) in DMF (80 mL) with K2CO3 (15.8 g, 1 14.32 mmol, 4.98 equiv) was added BnBr (5.8 g, 33.91 mmol, 1.48 equiv), and the reaction mixture was stirred at room temperature for 3 h. Water was added and the mixture was extracted with EtOAc thrice. The combined extracts were washed with brine and dried over Na2S04, then concentrated and purified by chromatography on silica gel (4:1 PE/EA) to yield 4-(benzyloxy)-1 -bromo-2-nitrobenzene as a light yellow solid.

 

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