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10250-59-6

10250-59-6 Structure

10250-59-6 Structure
IdentificationBack Directory
[Name]

1H-PRRAZOLE-5-CARBOXYLIC ACID ,1,3-DIMETHYL METHYL ESTER
[CAS]

10250-59-6
[Synonyms]

1,3-diMethyl-, Methyl ester
methyl 2,5-dimethylpyrazole-3-carboxylate
Methyl 2,5-dimethyl-2H-pyrazole-3-carboxylate
Methyl 1,3-diMethyl-1H-pyrazole-5-carboxylate
1,3-Dimethyl-1H-pyrazole-5-carboxylic acid methyl ester
2,5-dimethyl-2H-pyrazole-3-carboxylic acid methyl ester
Methyl 1,3-Dimethyl-1H-Pyrazole-5-Carboxylate(WXC00828)
1H-PRRAZOLE-5-CARBOXYLIC ACID ,1,3-DIMETHYL METHYL ESTER
1H-Pyrazole-5-carboxylic acid, 1,3-diMethyl-, Methyl ester
[Molecular Formula]

C7H10N2O2
[MDL Number]

MFCD06204177
[MOL File]

10250-59-6.mol
[Molecular Weight]

154.17
Chemical PropertiesBack Directory
[Boiling point ]

242.0±20.0 °C(Predicted)
[density ]

1.150 g/mL at 25 °C
[refractive index ]

n20/D1.491
[Fp ]

78℃
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

liquid
[pka]

0.94±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

NA 1993 / PGIII
[WGK Germany ]

1
[HS Code ]

2933199090
Hazard InformationBack Directory
[Uses]

Methyl 1,3-Dimethyl-1H-pyrazole-5-carboxylate is used as a reactant in the preparation of pyrazolyl acrylonitrile derivatives as acaricides.
[Synthesis]

5-METHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID METHYL ESTER

25016-17-5

Dimethyl sulfate

77-78-1

1H-PRRAZOLE-5-CARBOXYLIC ACID ,1,3-DIMETHYL METHYL ESTER

10250-59-6

1. dissolve methyl 5-methyl-1H-pyrazole-3-carboxylate (6.8 kg) in N,N-dimethylformamide (DMF, 8 L). 2. dimethyl sulfate (6.0 L) was slowly added dropwise over a period of 3 h. The rate of dropwise acceleration was controlled to maintain the reaction temperature at no more than 90°C. 3. After completion of the dropwise addition, the reaction mixture was heated and stirred at 80 °C for 18 hours. 4. After completion of the reaction, the mixture was cooled to room temperature, ice (3.4 kg) was added and further cooled in an ice bath. 5. 28% aqueous ammonium hydroxide solution (8.6 L) was slowly added to the reaction mixture over a period of 3 hours. 6. The resulting mixture was stirred for 18 hours and then diluted with ethyl acetate (12 L) and water (16 L), extracted and the organic layer was separated. 7. The organic layer was washed with water (4 L), dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the crude product of methyl 1,3-dimethyl-1H-pyrazole-5-carboxylate (5.14 kg, yield 69%, HPLC purity >90%). 8. The crude product was used directly in the subsequent reaction without further purification.

[References]

[1] Patent: WO2006/48761, 2006, A2. Location in patent: Page/Page column 33
[2] Journal of Agricultural and Food Chemistry, 2016, vol. 64, # 51, p. 9586 - 9591
Spectrum DetailBack Directory
[Spectrum Detail]

1H-PRRAZOLE-5-CARBOXYLIC ACID ,1,3-DIMETHYL METHYL ESTER(10250-59-6)1HNMR
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