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78242-20-3

78242-20-3 Structure

78242-20-3 Structure
IdentificationBack Directory
[Name]

1-Methyl-1H-pyrazol-4-ol
[CAS]

78242-20-3
[Synonyms]

1-methylpyrazol-4-ol
1-Methyl-1H-pyrazol-4-ol
1H-Pyrazol-4-ol, 1-methyl-
4-Hydroxy-1-methyl-1H-pyrazole
1-METHYL-1H-PYRAZOL-4-OL(WXC09189)
[Molecular Formula]

C4H6N2O
[MDL Number]

MFCD22414500
[MOL File]

78242-20-3.mol
[Molecular Weight]

98.1
Chemical PropertiesBack Directory
[Boiling point ]

217.7±13.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[pka]

9.19±0.14(Predicted)
[color ]

Cream
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261-P280
[HS Code ]

2933119000
Hazard InformationBack Directory
[Uses]

1-Methyl-1H-pyrazol-4-ol is used as a storage and transport stabiliser for polymerised compounds and as an intermediate in the preparation of pyrazole herbicides (1-methyl-5hydroxypyrazole).
[Synthesis]

1-Methyl-4-pyrazole boronic acid pinacol ester

761446-44-0

1-Methyl-1H-pyrazol-4-ol

78242-20-3

General procedure for the synthesis of 1-methyl-4-hydroxy-1H-pyrazole from 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole: To 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.0 g, 120.2 mmol) was added slowly, under the condition of 0 °C (ice bath cooling), to a 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole ( 25.0 g, 120.2 mmol) in tetrahydrofuran solution (600.9 mL, 0.2 M) was slowly added to aqueous sodium hydroxide solution (80.1 mL, 3 M, 240.3 mmol) followed by hydrogen peroxide (27.3 mL, 240.3 mmol). The reaction mixture was stirred at 0-25°C for 3 hours. After completion of the reaction, the reaction mixture was neutralized in a small heart with 12N hydrochloric acid (18.6 mL) and diluted with a solvent mixture of dichloromethane and methanol (90:10, 200 mL). The aqueous layer was extracted with a solvent mixture of dichloromethane and methanol (90:10, 3 x 200 mL). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to afford the target product 1-methyl-4-hydroxy-1H-pyrazole.

[References]

[1] Tetrahedron Letters, 2017, vol. 58, # 49, p. 4587 - 4590
[2] Patent: WO2016/11930, 2016, A1. Location in patent: Page/Page column 138
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 4, p. 1370 - 1387
Spectrum DetailBack Directory
[Spectrum Detail]

1-Methyl-1H-pyrazol-4-ol(78242-20-3)1HNMR
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