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Chemical Structure| 409082-11-7 Chemical Structure| 409082-11-7

Structure of 409082-11-7

Chemical Structure| 409082-11-7

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Product Details of [ 409082-11-7 ]

CAS No. :409082-11-7
Formula : C9H8N2O2
M.W : 176.17
SMILES Code : CC1=C(CC#N)C=C(C=C1)[N+]([O-])=O
MDL No. :MFCD09835002

Safety of [ 409082-11-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 409082-11-7 ]

* 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 [ 409082-11-7 ]

[ 409082-11-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 409082-11-7 ]
  • [ 287119-83-9 ]
YieldReaction ConditionsOperation in experiment
With methanol; potassium hydroxide; water; for 14h;Heating / reflux; 2-(2-Methyl-5-nitrophenyl)ethanenitrile 12 (87 g, 494 mmol) is dissolved in methanol : water = 1 : 1 (1.2 L). Potassium hydroxide (277 g, 4.94 mol) in water (1 L) is added and the reaction is heated at reflux for 14 h. After cooling to rt and removing the methanol in vacuo, the aqueous layer is washed with DCM and ether. The combined organic layer is washed with brine, dried over sodium sulfate, and filtered. After removing the solvent in vacuo, the product 13 is obtained as an orange solid. 1H NMR (300MHz, CDCl3) delta 8.07 (m, 2H), 7.35 (d, J= 8.1 Hz, IH), 3.78 (s, 2H), 2.43 (s, 3H).
With water; potassium hydroxide; In methanol; for 14h;Reflux; [00124] 2-(2-Methyl-5-nitrophenyl)ethanenitrile 12 (87 g, 494 mmol) was dissolved in methanol : water = 1 : 1 (1.2 L). Potassium hydroxide (277 g, 4.94 mol) in water (1 L) was added and the reaction was heated at reflux for 14 h. After cooling to rt and removing the methanol in vacuo, the aqueous layer was washed with DCM and ether. The combined organic layer was washed with brine, dried over sodium sulfate, and filtered. After removing the solvent in vacuo, the product 13 was obtained as an orange solid. 1H NMR (300MHz, CDCI3) delta 8.07 (m, 2H), 7.35 (d, J= 8.1 Hz, IH), 3.78 (s, 2H), 2.43 (s, 3H).
With potassium hydroxide; water; In methanol; for 14h;Heating / reflux; 2- (2-methyl-5-nitrophenyl)-ethanenitrile (2. 5g, 14. 2mmol) is dissolved in 50mL methanol. Potassium hydroxide (8. 0g, 142mmol) in 50mL water is added and the reaction is heated to reflux for 14 hours. After cooling down and removing the methanol, the aqueous layer is washed with DCM and ether. The combined organic layer is washed with brine and dried over sodium sulfate and filtered. After removing the solvent under the vacuum, the final product compound (15) 2- (2-methyl-5-nitrophenyl)-acetic acid is the orange solid, 1. 9g.
 

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