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38993-84-9

38993-84-9 Structure

38993-84-9 Structure
IdentificationBack Directory
[Name]

(1-METHYL-1H-IMIDAZOL-5-YL)METHANOL
[CAS]

38993-84-9
[Synonyms]

RARECHEM AL BD 0940
1-Methyl-5-imidazolemethanol
(3-methylimidazol-4-yl)methanol
1-Methyl-1H-imidazole-5-methanol
1H-Imidazole-5-methanol,1-methyl-
5-(HydroxyMethyl)-1-MethyliMidazole
(1-METHYL-1H-IMIDAZOL-5-YL)METHANOL
1-METHYL-5-(HYDROXYMETHYL)IMIDAZOLE
(3-METHYL-3H-IMIDAZOL-4-YL)-METHANOL
5-HYDROXYMETHYL-1-METHYL-1H-IMIDAZOLE
[Molecular Formula]

C5H8N2O
[MDL Number]

MFCD02179522
[MOL File]

38993-84-9.mol
[Molecular Weight]

112.13
Chemical PropertiesBack Directory
[Melting point ]

113 °C
[Boiling point ]

324.9±17.0 °C(Predicted)
[density ]

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

Inert atmosphere,Room Temperature
[solubility ]

DMSO (Sparingly), Methanol (Slightly)
[form ]

Solid
[pka]

14.35±0.10(Predicted)
[color ]

Pale Yellow
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

36/37/38-22
[Safety Statements ]

26-36/37/39-37/39-36
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933299090
Spectrum DetailBack Directory
[Spectrum Detail]

(1-METHYL-1H-IMIDAZOL-5-YL)METHANOL(38993-84-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-METHYL-1H-IMIDAZOLE-5-CARBOXALDEHYDE

39021-62-0

(1-METHYL-1H-IMIDAZOL-5-YL)METHANOL

38993-84-9

General procedure for the synthesis of 1-methyl-1H-imidazol-5-yl)methanol from 1-methyl-1H-5-formyl-imidazole: 1-methyl-1H-5-formyl-imidazole (4.0 g, 15 mmol) was suspended in tetrahydrofuran (THF) (10 mL) and the resulting solution was cooled to 0 °C. Lithium aluminum hydride (300 mg, 32.0 mmol) was added in batches over 10 min and the resulting suspension was continued to be stirred for 10 min. Under vigorous stirring, the excess hydride was quenched by bulk addition of solid Na2SO4-10H2O (~1 g). Additional THF was added as needed to prevent the slurry from solidifying. The resulting suspension was continued to be stirred for 1 h. Subsequent filtration to remove the sulfate and solvent removal under reduced pressure afforded the target alcohol (1.3 g, 80% yield).1H NMR (400 MHz, CD3OD): δ 7.57 (s, 1H), 6.89 (s, 1H), 4.58 (s, 2H), 3.72 (s, 3H).13C NMR (100 MHz. CD3OD): δ140.1,132.7,128.1,31.9,31.0.

[References]

[1] Journal of Medicinal Chemistry, 2006, vol. 49, # 19, p. 5710 - 5727
[2] Patent: WO2006/102159, 2006, A2. Location in patent: Page/Page column 22
[3] Journal of the American Chemical Society, 1949, vol. 71, p. 2444,2447
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