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Chemical Structure| 90005-90-6 Chemical Structure| 90005-90-6

Structure of 90005-90-6

Chemical Structure| 90005-90-6

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Product Details of [ 90005-90-6 ]

CAS No. :90005-90-6
Formula : C8H9NO3
M.W : 167.16
SMILES Code : OC1=CC([N+]([O-])=O)=CC=C1CC

Safety of [ 90005-90-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H315-H319-H412
Precautionary Statements:P501-P273-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 90005-90-6 ]

* 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 [ 90005-90-6 ]

[ 90005-90-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20191-74-6 ]
  • [ 90005-90-6 ]
YieldReaction ConditionsOperation in experiment
52% Step3. A solution of sulfuric acid (98percent, 39 g, 390.00 mmol) in water (160 mL) was added to <strong>[20191-74-6]2-ethyl-5-nitrobenzenamine</strong> (12.9 g, 69.94 mmol, prepared as described in Step 2 above). The mixture was cooled to 0-5 0C, and a solution of sodium nitrite (5.63 g, 81.59 mmol) in water (20 mL) was then added. The resulting solution was maintained for 30 min at 0-5 0C. Sulfuric acid (65percent, 600 g, 3.98 mol) was then added, and the temperature was maintained at reflux for 1 hr. The reaction mixture was cooled in a bath of iced water, and the product was extracted with ethyl acetate. The organic layers were combined and washed with aqueous saturated sodium bicarbonate and brine (200 mL). The solution was dried (anhydrous MgSO-i), filtered, and concentrated. The residue was purified by eluting through a column with a 1 :10 (v/v) ethyl acetate/petroleum ether solvent system to afford 7.65 g (52 percent yield) of 2-ethyl-5-nitrophenol as a red solid.
With sulfuric acid; water; sodium nitrite; at 0 - 5℃; for 1.5h;Heating / reflux; Step 3; A solution of sulfuric acid (98percent, 39 g, 390.00 mmol) in water (160 mL) was added to <strong>[20191-74-6]2-ethyl-5-nitrobenzenamine</strong> (12.9 g, 69.94 mmol, prepared as described in Step 2 <n="55"/>above). The mixture was cooled to 0-5 0C5 and a solution of sodium nitrite (5.63 g, 81.59 mmol) in water (20 mL) was then added. The resulting solution was maintained for 30 minutes at 0-5 0C. Sulfuric acid (65percent, 600 g, 3.98 mol) was then added, and the temperature was maintained at reflux for 1 hr. The reaction mixture was cooled in a bath of iced water, and the product was extracted with ethyl acetate. The organic layers were combined and washed with aqueous saturated sodium bicarbonate and brine. The solution was dried (MgSO-j), filtered and concentrated. The residue was purified by eluting through a column with a 1 : 10 ethyl acetate/petroleum ether solvent system to afford 7.65 g of 2-ethyl-5-nitrophenol as a red solid.
 

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