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Chemical Structure| 58586-81-5 Chemical Structure| 58586-81-5

Structure of 58586-81-5

Chemical Structure| 58586-81-5

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Product Details of [ 58586-81-5 ]

CAS No. :58586-81-5
Formula : C9H12N2O2
M.W : 180.20
SMILES Code : O=C(NN)C1=CC=C(OCC)C=C1
MDL No. :MFCD00017074

Safety of [ 58586-81-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 58586-81-5 ]

* 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 [ 58586-81-5 ]

[ 58586-81-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 92-55-7 ]
  • [ 58586-81-5 ]
  • 4-ethoxy-N’-((5-nitrofuran-2-yl)methylene)benzohydrazide [ No CAS ]
  • 2
  • [ 23676-08-6 ]
  • [ 58586-81-5 ]
YieldReaction ConditionsOperation in experiment
95.4% With hydrazine hydrate; In methanol; for 0.0833333h;Microwave irradiation; General procedure: The benzoic acid hydrazides, 3a-h were prepared accordingto reported method in literature28,29 with some desirablemodifications. The ester (2a-h, 0.1 mol) dissolved inappropriate volume of methanol was transferred to a flaskwith a reflux condenser. Hydrazine hydrate (99%, 0.15 mol) was slowly added to the mixture and then kept on reflux forabout 5-6 h. The excess of solvent and hydrazine hydratewere distilled off. On addition of water the product separatedout which was washed several times with distilled water anddried. The product was recrystallized from 80% aqueous ethanoland melting points determined (Table 2).Microwave method: The same procedure as stated abovewas adopted using 100 ml methanol following the other conditionsof microwave in a microwave reactor at 350 Watt(power) for 3-5 min. Precipitation and separation of precipitatewas done as for conventional method (Table 2).
With hydrazine hydrate; In water; at 75℃; for 0.166667h; General procedure: Hydrazine hydrate 64% (v/v) (30.0 mL, 0.33 mol) was heated up to 50-60 C. The methyl ester 3 (0.01 mol) was added and the mixture was heated at reflux for 10 min. The cooling was performed sequentially in water bath, followed by ice bath and dry ice-ethanol bath. The precipitate was filtered and washed with cold water.
With hydrazine hydrate; In methanol; at 10 - 80℃; for 6h; General procedure: 13.5 mmol of the methyl benzoate derivatives were added to 100 mL of methanol at the 250 mL double-mouth bottle. Add 6.75 mL (108 mmol) of hydrazine hydrate to the reactive mixture gradually between 10 and 25 C over 2 h. Then the temperature increased to 80 C and refluxed for 4 h, subsequently lowered to room temperature. After the methanol is removed by decompression concentration, 300 mL of added water was mixed at 5 C to decrystallize, and the white solid (b) is obtained by filtration and drying.
 

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