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Chemical Structure| 879-57-2 Chemical Structure| 879-57-2

Structure of 879-57-2

Chemical Structure| 879-57-2

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Product Details of [ 879-57-2 ]

CAS No. :879-57-2
Formula : C9H12N2O2
M.W : 180.20
SMILES Code : N=C(NO)C1=CC=CC=C1OCC

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Application In Synthesis of [ 879-57-2 ]

* 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 [ 879-57-2 ]

[ 879-57-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 6609-57-0 ]
  • [ 879-57-2 ]
YieldReaction ConditionsOperation in experiment
97% With hydroxylamine; In ethanol; water; at 50℃; for 12h; Hydroxylamine (Fluka 55458; 50% in water; 4.08 ml 67.95 mmol; 5 eq.) was added to a solution of <strong>[6609-57-0]2-ethoxybenzonitrile</strong> (Fluorochem 18661 ; 2 g; 13.59 mmol; 1 eq.) in EtOH (30 ml.) and the reaction mixture was stirred at 5O0C for 12 hours. Evaporation in vacuo gave a white solid, which was further dried under high vaccum to afford the title compound (2.38 g: 97%) as a white solid.HPLC (Method A) : Rt 1.22 min (purity 98.2%). LC/MS : 181.0 (M+H)+.
90% With hydroxylamine hydrochloride; potassium carbonate; In ethanol; for 4h;Reflux; Add 97% in a 250mL four-necked bottleCompound IV 15.2g (0.1mol),9g (0.13mol) of hydroxylamine hydrochloride,17.9g (0.13mol) was added to 100mL of ethanol,The reaction was refluxed for 4 h.TLC traces the reaction to Compound IV completely, drops to room temperature, and removes the potassium salt in the reaction solution by filtration.The filtrate was evaporated to 80% ethanol, and a white solid precipitated upon cooling.Filter by suction and recover the filtrate.A white solid was obtained in an amount of 16.2 g, yield 90%.
89% With hydroxylamine hydrochloride; triethylamine; In ethanol; at 50 - 60℃; for 2h;Reflux; To a 250 mL three-necked flask, 100 mL of ethanol, 13.8 g (0.2 mol) of hydroxylamine hydrochloride and 20 g (0.2 mol) of triethylamine were added, and the mixture was heated to 50-60 C for 1 h, and free hydroxylamine hydrochloride. After 1 h, 18 g of compound 4 (<strong>[6609-57-0]o-ethoxybenzonitrile</strong>) was added to the flask, and the mixture was refluxed for 2 h. The compound 4 disappeared by TLC. Ethanol was distilled off, and 150 mL of water was added to the flask to dissolve the triethylamine hydrochloride. The mixture was filtered under suction, and the cake was compound 3, which was dried to give a white solid.
 

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