Basic information Uses Safety Supplier Related

3H-PYRAZOL-3-ONE, 1,2-DIHYDRO-

Basic information Uses Safety Supplier Related

3H-PYRAZOL-3-ONE, 1,2-DIHYDRO- Basic information

Product Name:
3H-PYRAZOL-3-ONE, 1,2-DIHYDRO-
Synonyms:
  • 1,2-dihydropyrazol-3-one
  • 1,2-Dihydro-3H-pyrazol-3-one
  • 1,2-dihydropyrazol-3-on
  • Pyrazol-5-ol
  • Pyrazol-3-ol
  • NSC 520837
  • 4-Pyrazolin-3-one
  • 3-Pyrazolone
CAS:
137-45-1
MF:
C3H4N2O
MW:
84.08
Mol File:
137-45-1.mol
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3H-PYRAZOL-3-ONE, 1,2-DIHYDRO- Chemical Properties

Melting point:
160-162 °C
Density 
1.191±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
9.00±0.70(Predicted)
form 
solid
color 
Pale yellow
InChI
InChI=1S/C3H4N2O/c6-3-1-2-4-5-3/h1-2H,(H2,4,5,6)
InChIKey
XBYRMPXUBGMOJC-UHFFFAOYSA-N
SMILES
N1C=CC(=O)N1
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Safety Information

HS Code 
2933199090
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3H-PYRAZOL-3-ONE, 1,2-DIHYDRO- Usage And Synthesis

Uses

1,2-Dihydro-3H-pyrazole-3-one, also known as 1H-pyrazole-3(2H)-one, is an organic intermediate that can be prepared by one-step cyclization from methyl propargylate, ethyl acrylate, or (2E)-3-methoxyacrylate.

Synthesis

922-67-8

137-45-1

General procedure for the synthesis of 1,2-dihydro-3H-pyrazol-3-one from methyl propargylate: Hydrazine hydrate (3.62 mL, 48.53 mmol) was slowly added dropwise to a solution of methyl propargylate (4.23 mL, 47.58 mmol) dissolved in methanol (40 mL) under cooling conditions in an ice bath. The reaction mixture was stirred at room temperature for 30 min. Subsequently, brine (10 mL) was added and methanol was removed by distillation under reduced pressure. The remaining aqueous layer was extracted with ethyl acetate (4 × 75 mL), the organic layers were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1,2-dihydro-3H-pyrazol-3-one (3.82 g, 95% yield) as a milky white solid. Nuclear magnetic resonance hydrogen spectrum (400 MHz, DMSO-d6): δ 5.44 (1H, d, J = 2.27 Hz), 7.35 (1H, d, J = 2.23 Hz), 9.50 (1H, br s, NH), 11.45 (1H, br s, NH); nuclear magnetic resonance carbon spectrum (101 MHz, DMSO-d6): δ 89.25, 129.71, 160.73; MS (electrospray positive ionization mode): m/z 85.04 (100, [M+H]+); high-resolution MS (electrospray ionization): measured value of [M+H]+ 85.03951, calculated value of C3H5N2O 85.03964.

References

[1] Tetrahedron, 2012, vol. 68, # 27-28, p. 5434 - 5444
[2] Patent: US2016/376287, 2016, A1. Location in patent: Paragraph 0634
[3] Patent: WO2017/117708, 2017, A1. Location in patent: Paragraph 54

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