ChemicalBook--->CAS DataBase List--->84547-62-6

84547-62-6

84547-62-6 Structure

84547-62-6 Structure
IdentificationBack Directory
[Name]

(1-Methyl-1H-pyrazol-3-yl)methanol
[CAS]

84547-62-6
[Synonyms]

84547-62-6
AKOS PAO-1076
(1-methyl-3-pyrazolyl)methanol
(1-methylpyrazol-3-yl)methanol
1-Methyl-1H-pyrazole-3-methanol
1H-Pyrazole-3-Methanol, 1-Methyl-
(1-METHYL-1H-PYRAZOL-3-YL)METHANOL
(1-methyl-1h-pyrazole-3-yl) methanol
3-(Hydroxymethyl)-1-methyl-1H-pyrazole
(1-Methyl-1H-pyrazol-3-yl)methanol90+%
3-(Hydroxymethyl)-1-methyl-1H-pyrazole95%
3-(Hydroxymethyl)-1-methyl-1H-pyrazole 95%
3-(Hydroxymethyl)-1-methyl-1H-pyrazole 90+%
(1-Methyl-1H-Pyrazol-3-Yl)Methanol(WX640316)
[Molecular Formula]

C5H8N2O
[MDL Number]

MFCD08690274
[MOL File]

84547-62-6.mol
[Molecular Weight]

112.13
Chemical PropertiesBack Directory
[Boiling point ]

243.6±15.0 °C(Predicted)
[density ]

1.16±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.61±0.10(Predicted)
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Note ]

Harmful
[HS Code ]

2933199090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Tetrahydrofuran-->N,N-Dimethylformamide-->n-Butyllithium-->Nitrogen-->Sodium borohydride-->1-Methylpyrazole-->1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE-->methyl 1-methyl-1H-pyrazole-3-carboxylate-->Lithium Aluminum Hydride
[Preparation Products]

5-(Hydroxymethyl)-1-methyl-1H-pyrazole-->1-METHYL-1H-PYRAZOLE-3-CARBALDEHYDE
Spectrum DetailBack Directory
[Spectrum Detail]

(1-Methyl-1H-pyrazol-3-yl)methanol(84547-62-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 1-methyl-1H-pyrazole-3-carboxylate

17827-61-1

(1-Methyl-1H-pyrazol-3-yl)methanol

84547-62-6

General procedure for the synthesis of (1-methyl-1H-pyrazol-3-yl)methanol from methyl 1-methyl-1H-pyrazole-3-carboxylate: lithium aluminium hydride (11.9 g, 314.29 mmol) was added batchwise to methyl 1-methyl-1H-pyrazole-3-carboxylate (22.0 g, 157.14 mmol) in a tetrahydrofuran (150 mL) at 0-5 °C solution. Subsequently, the reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the reaction mixture was cooled to 0 °C using a water/ice bath and 15 mL of water was added to quench the reaction. The resulting solution was diluted with 200 mL of dichloromethane and dried with anhydrous sodium sulfate. After filtration to remove the solid, the mixture was concentrated under vacuum to give (1-methyl-1H-pyrazol-3-yl)methanol as a light yellow liquid (6.0 g, 35% yield).

[References]

[1] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[2] Journal of the Chemical Society, Chemical Communications, 1985, # 24, p. 1765 - 1766
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