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(1H-Pyrazol-3-yl)methanol

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(1H-Pyrazol-3-yl)methanol Basic information
Product Name:(1H-Pyrazol-3-yl)methanol
Synonyms:3-(HYDROXYMETHYL)PYRAZOLE;1H-PYRAZOLE-3-METHANOL;1H-pyarzole-3-methanol;3-HyroxyMethyl-1H-pyrazole;3-HyroxyMethyl-1H-pyrazol...;1H-Pyrazole-3-methanol (9CI, ACI);1H-Pyrazole-3-methanol 95%;3-(Hydroxymethyl)pyrazole , (1H-Pyrazol-3-yl)methanol
CAS:23585-49-1
MF:C4H6N2O
MW:98.1
EINECS:
Product Categories:pharmacetical
Mol File:23585-49-1.mol
(1H-Pyrazol-3-yl)methanol Structure
(1H-Pyrazol-3-yl)methanol Chemical Properties
Melting point 184-185 °C
Boiling point 137-140 °C(Press: 0.5 Torr)
density 1.225 g/cm3(Temp: 25 °C)
storage temp. 2-8°C
form solid
pka13.59±0.10(Predicted)
color Off White
Safety Information
HS Code 2933119000
MSDS Information
(1H-Pyrazol-3-yl)methanol Usage And Synthesis
Chemical PropertiesColorless Liquid
Synthesis
5-Pyrazolecarboxylic acid

1621-91-6

(1H-PYRAZOL-3-YL)METHANOL

23585-49-1

General procedure for the synthesis of 3-(hydroxymethyl)pyrazole from 1H-pyrazole-3-carboxylic acid: a tetrahydrofuran solution (20 mL) of aluminum (III) hydride was cooled to 0 °C under nitrogen protection and stirred. To this solution was added 1H-pyrazole-3-carboxylic acid (4 g, 35.7 mmol). The reaction mixture was stirred at room temperature for 1 hour and then heated to reflux overnight. Upon completion of the reaction, the mixture was cooled to 0 °C and water (2.7 mL), 10% NaOH solution (5.4 mL) and water (8.1 mL) were added sequentially to quench the reaction. After quenching, the mixture was continued to be stirred at 0 °C for 30 min and then filtered through a Celite pad. The filtrate was concentrated under reduced pressure to remove the solvent and the resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1/2, v/v) to afford the target product (1H-pyrazol-3-yl)methanol (1.9 g, 19.37 mmol, 54% yield) as a buttery solid. m/z = 81.1 [M + H - H2O]+ was shown by LCMS detection.

References[1] Patent: WO2017/216726, 2017, A1. Location in patent: Page/Page column 968
[2] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
(1H-Pyrazol-3-yl)methanol Preparation Products And Raw materials
Raw materialsPropargyl alcohol-->5-Pyrazolecarboxylic acid-->(Trimethylsilyl)diazomethane-->Lithium Aluminum Hydride-->Tetrahydrofuran
Preparation Products(1H-Pyrazol-4-yl)methanol
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