ChemicalBook--->CAS DataBase List--->85230-37-1

85230-37-1

85230-37-1 Structure

85230-37-1 Structure
IdentificationBack Directory
[Name]

Ethyl 5-Oxo-4,5-dihydro-1H-pyrazole-3-carboxylate
[CAS]

85230-37-1
[Synonyms]

EOS-61141
Ethyl 5-hydroxy-1H-pyrazole-3-carboxylate
Ethyl 5-Oxo-4,5-dihydro-1H-pyrazole-3-carboxylate
1H-Pyrazole-3-carboxylic acid, 5-hydroxy-, ethyl ester
[Molecular Formula]

C6H8N2O3
[MDL Number]

MFCD00020698
[MOL File]

85230-37-1.mol
[Molecular Weight]

156.14
Chemical PropertiesBack Directory
[Melting point ]

137-138 °C
[Boiling point ]

400.1±25.0 °C(Predicted)
[density ]

1.371±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

7.96±0.23(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C6H8N2O3/c1-2-11-6(10)4-3-5(9)8-7-4/h3H,2H2,1H3,(H2,7,8,9)
[InChIKey]

FGCPAXRNQIOISG-UHFFFAOYSA-N
[SMILES]

N1C(O)=CC(C(OCC)=O)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P501-P264-P280-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405
[HS Code ]

2933199090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 5-Oxo-4,5-dihydro-1H-pyrazole-3-carboxylate(85230-37-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Diethyl oxalacetate sodium salt

40876-98-0

Ethyl  5-Oxo-4,5-dihydro-1H-pyrazole-3-carboxylate

85230-37-1

The general procedure for the synthesis of ethyl 5-keto-4,5-dihydro-1H-pyrazole-3-carboxylate from the sodium salt of diethyl oxaloacetate was as follows: acetic acid (150 mL) was slowly added dropwise to a solution of 1,4-diethoxy-1,4-dioxobut-2-en-2-ol (30.0 g, 0.143 mol) in toluene (150 mL). The reaction mixture was stirred at room temperature for 30 minutes before 85% hydrazine hydrochloride (17 g, 0.29 mol) was added. Stirring was continued at room temperature for 30 minutes, after which the reaction system was heated to 100 °C and kept overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and extracted with ethyl acetate (500 mL). The organic phase was washed sequentially with saturated aqueous sodium bicarbonate (200 mL) and saturated aqueous sodium chloride (200 mL), dried over anhydrous sodium sulfate and filtered, and concentrated under reduced pressure to give a yellow solid product. The yield was 17 g (0.11 mol) with 77% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 12.75 (br s, 1H), 5.91 (br s, 1H), 4.24 (q, J = 7 Hz, 2H), 1.27 (t, J = 7 Hz, 3H).

[References]

[1] Patent: WO2017/145013, 2017, A1. Location in patent: Page/Page column 54
[2] Chemical and Pharmaceutical Bulletin, 1983, vol. 31, # 4, p. 1228 - 1234
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