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Chemical Structure| 1313372-75-6 Chemical Structure| 1313372-75-6

Structure of 1313372-75-6

Chemical Structure| 1313372-75-6

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Product Details of [ 1313372-75-6 ]

CAS No. :1313372-75-6
Formula : C8H7N3O2
M.W : 177.16
SMILES Code : O=[N+](C1=CC2=NNC(C)=C2C=C1)[O-]
MDL No. :MFCD18633573
InChI Key :FUNWSYKLFDLUIZ-UHFFFAOYSA-N
Pubchem ID :10921054

Safety of [ 1313372-75-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1313372-75-6 ]

* 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 [ 1313372-75-6 ]

[ 1313372-75-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 20191-74-6 ]
  • [ 1313372-75-6 ]
YieldReaction ConditionsOperation in experiment
95.7% With tert.-butylnitrite; acetic acid; at 20℃; for 1h; Tert-Butyl nitrite (25 ml, 0.15 mol)Of glacial acetic acid (100 ml)The solution was dropped to 2 (25 g, 0.15 mol)In glacial acetic acid (500 ml).The reaction was continued with stirring1h.After completion of the reaction, the reaction solution was concentrated to dryness,The resulting solid was dissolved in ethyl acetate (250 ml)The reaction mixture was washed successively with saturated aqueous sodium hydrogencarbonate (125 ml x 3)Saturated brine (50 ml)The solvent was distilled off under reduced pressure,Yielding yellow solid 3 (25.5 g, 95.7percent)
77.4% <strong>[20191-74-6]2-ethyl-5-nitroaniline</strong> (1.03g, 6.2mmol, 1 equiv) was dissolved in glacial acetic acid (30ml) at room temperature under nitrogen. Tert-butylnitrite (0.9ml, 7.5ml, 1.2equiv) in glacial <n="35"/>acetic acid (16ml) was added drop wise over 20 min. The reaction was stirred for 30 min and the acid was removed under vacuum to give an orange solid. The solid was taken up in ethyl acetate (50ml) and washed with saturated sodium bicarbonate solution (3 x 50ml). The organics layers were dried over magnesium sulphate and concentrated to yield the desired compounds as of a brown solid (0.85g, 77.4percent).1H NMR (CDCl3, 400MHz) delta= 9.67, (br s, IH), 8.36 (d, J = 2Hz5 IH), 7.95 (dd, J = 2Hz, J = 9Hz, IH), 7.73 (d, J = 9Hz, IH), 2.70 (s, 3H).
  • 2
  • [ 1313372-75-6 ]
  • [ 444731-75-3 ]
 

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