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Chemical Structure| 782501-73-9 Chemical Structure| 782501-73-9

Structure of 782501-73-9

Chemical Structure| 782501-73-9

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Product Details of [ 782501-73-9 ]

CAS No. :782501-73-9
Formula : C8H12N2O3
M.W : 184.19
SMILES Code : O=C(C1=CNN=C1)OC(CCO)C

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Application In Synthesis of [ 782501-73-9 ]

* 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 [ 782501-73-9 ]

[ 782501-73-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109-84-2 ]
  • [ 80370-42-9 ]
  • [ 782501-73-9 ]
YieldReaction ConditionsOperation in experiment
96% In ethanol; at 0 - 20℃; for 48h; [00269] Step A: A solution of 2-hydrazinylethanol (2.76 g, 32.7 mmol) in EtOH (10 mL) was added dropwise to a solution of <strong>[80370-42-9]ethyl 2-formyl-3-oxopropanoate</strong> (4.71 g, 32.7 mmol, prepared as described in Bertz, Steven H., et al. "New preparations of ethyl 3,3- diethoxypropionate and ethoxycarbonylmalondialdehyde. Copper(I) catalyzed acetal formation from a conjugated triple bond." J. Org. Chem. Vol. 47 (1982): pp. 2216-2217) in EtOH (20 mL) at O0C. The reaction mixture was stirred at room temperature for 48 hours and then concentrated to give ethyl l-(2-hydroxyethyl)-lH-pyrazole-4-carboxylate (5.8 g, 31.5 mmol, 96percent yield) as an oil. m/z (APCI-pos) M+l = 185.1.
95% In ethanol; at 0 - 20℃; Compound 5 was prepared using the classical approach for preparing pyrazoles [7]. Ethyl 2-formyl-3-oxopropionate (2.80 g; 20 mmol) was dissolved in 20 ML of ethanol and cooled to 0°C. 2-Hydroxyethylhydrazine (1.44 g; 20 mmol) was dissolved in 100 ml of ethanol and was added dropwise to the solution of ethyl 2-FORMYL-3-OXOPROPIONATE. The reaction mixture was left overnight at room temperature. The solvent was vacuum removed yielding a yellow oil. Yield: 95percent H-NMR (CDC13) : 7.93 (s, H (3) pz, 1H) ; 7. 91 (s, H (5) pz, 1H) ; 4.30-4. 22 (m, CH2+OCH2, 5H); 3.99 (t, CH2,2H) ; 1.30 (t, CH3, 3H).
 

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