Basic information Application Safety Supplier Related

(1-METHYL-1H-IMIDAZOL-4-YL)METHANOL

Basic information Application Safety Supplier Related

(1-METHYL-1H-IMIDAZOL-4-YL)METHANOL Basic information

Product Name:
(1-METHYL-1H-IMIDAZOL-4-YL)METHANOL
Synonyms:
  • (1-METHYL-1H-IMIDAZOL-4-YL)METHANOL
  • 1-Methyl-4-imidazolemethanol
  • 4-(Hydroxymethyl)-1-methylimidazole
  • (1-Methyl-1H-imidazol-4-yl)methanol97%
  • (1-Methyl-1H-imidazol-4-yl)methanol 97%
  • 1H-Imidazole-4-methanol, 1-methyl-
  • (1-methylimidazol-4-yl)methanol
CAS:
17289-25-7
MF:
C5H8N2O
MW:
112.13
Mol File:
17289-25-7.mol
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(1-METHYL-1H-IMIDAZOL-4-YL)METHANOL Chemical Properties

Melting point:
59.5-63.5
Boiling point:
324.9±17.0 °C(Predicted)
Density 
1.16±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
13.61±0.10(Predicted)
Appearance
Light yellow to brown Solid
InChI
InChI=1S/C5H8N2O/c1-7-2-5(3-8)6-4-7/h2,4,8H,3H2,1H3
InChIKey
NLEAEGDBKRBJAP-UHFFFAOYSA-N
SMILES
C1N(C)C=C(CO)N=1
CAS DataBase Reference
17289-25-7
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Safety Information

Hazard Note 
Harmful
HS Code 
2933299090
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(1-METHYL-1H-IMIDAZOL-4-YL)METHANOL Usage And Synthesis

Application

(1-Methyl-1H-imidazol-4-yl)methanol is an organic intermediate that can be obtained by reducing 1-methyl-imidazol-4-carboxylic acid. It can be further chlorinated to prepare 1-methyl-4-chloromethylimidazolium hydrochloride. As an organic synthesis intermediate and pharmaceutical intermediate, it can be used in laboratory research and development processes and chemical production processes.

Synthesis

41716-18-1

17289-25-7

General procedure for the synthesis of (1-methyl-1H-imidazol-4-yl)methanol from 1-methyl-1H-imidazole-4-carboxylic acid: 1-methyl-1H-imidazole-4-carboxylic acid (25 g, 198 mmol) was dissolved in tetrahydrofuran (THF) (1000 mL) under nitrogen protection. Lithium aluminum hydride (LiAlH4) (15.05 g, 396 mmol) was added slowly at room temperature. The reaction mixture was stirred at 50 °C for 12 hours. Upon completion of the reaction, water (15 mL), 10% sodium hydroxide solution (15 mL), and water (45 mL) were sequentially added to the reaction mixture at 0 °C. The solid was removed by filtration and the filtrate was concentrated to afford the target product (1-methyl-1H-imidazol-4-yl)methanol (13.2 g, 94 mmol, 47.5% yield), which could be used in the next step of the reaction without further purification.LC-MS analysis result: m/z 113.1 ([M + H]+), retention time 0.33 min.

References

[1] Patent: WO2004/13134, 2004, A2. Location in patent: Page 26
[2] Patent: WO2004/13135, 2004, A1. Location in patent: Page 47
[3] Patent: WO2004/16606, 2004, A1. Location in patent: Page 30
[4] Patent: WO2004/13138, 2004, A2. Location in patent: Page 23
[5] Patent: WO2017/60854, 2017, A1. Location in patent: Page/Page column 474; 475

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