3-bromo-1-methyl-1H-pyrazole Chemical Properties

Density 

1.585 g/mL at 25 °C

refractive index 

n20/D1.528

Flash point:

106℃

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

form 

liquid

pka

-0.27±0.10(Predicted)

Appearance

Colorless to light yellow Liquid

Boiling point:

204-210°C/760 mmHg

InChI

InChI=1S/C4H5BrN2/c1-7-3-2-4(5)6-7/h2-3H,1H3

InChIKey

ZGEVJEQMVRIEPX-UHFFFAOYSA-N

SMILES

N1(C)C=CC(Br)=N1

Safety Information

RIDADR 

UN 2811 6.1 / PGIII

WGK Germany 

3

HS Code 

2933199090

3-bromo-1-methyl-1H-pyrazole Usage And Synthesis

Uses

3-bromo-1-methyl-1H-pyrazole is mainly used in chemical manufacturing or organic synthesis. Due to its structural properties it can be used for regioselective synthesis.

Synthesis

General procedure for the synthesis of 3-bromo-1-methylpyrrole from N-methyl-3-aminopyrazole: A) Synthesis of 3-bromo-1-methyl-1H-pyrazole: To a solution of 1-methyl-1H-pyrazol-3-amine (2.00 g) in hydrobromic acid (14.0 mL) was added slowly and dropwise to an aqueous solution (2.06 mL) of sodium nitrite (1.56 g) under the cooling of an ice bath. The reaction mixture was stirred under ice bath cooling for 30 minutes before a solution of copper(I) bromide (7.39 g) in hydrobromic acid (14.0 mL) was slowly added. The reaction mixture was continued to be stirred under ice bath cooling for 30 hours. Upon completion of the reaction, the reaction solution was neutralized with saturated aqueous sodium bicarbonate and diluted with dichloromethane. The insoluble material was removed by filtration, and the filtrate was washed sequentially with water and saturated brine and dried over anhydrous magnesium sulfate. After evaporation of the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford 3-bromo-1-methylpyrrole (818 mg). The product was characterized by 1H NMR (400 MHz, CDCl3): δ3.88 (3H, s), 6.25 (1H, d, J=2.4 Hz), 7.25 (1H, d, J=2.0 Hz).

References

[1] Journal of Organic Chemistry, 1991, vol. 56, # 22, p. 6313 - 6320
[2] Patent: EP2818473, 2014, A1. Location in patent: Paragraph 0577
[3] Synthesis (Germany), 2015, vol. 47, # 5, p. 679 - 691

3-bromo-1-methyl-1H-pyrazole(151049-87-5)Related Product Information

• 1-Methylpyrazole
• 3,4,5-TRIBROMO-1-(4-NITROPHENYL)-1H-PYRAZOLE
• 4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ANILINE
• N-(2-FLUOROBENZOYL)-N'-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]UREA
• DIETHYL 2-([4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ANILINO]METHYLIDENE)MALONATE
• 2-([4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ANILINO]METHYLIDENE)MALONONITRILE
• N1-[2-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ETHYL]-4-CHLOROBENZAMIDE
• N-(4-CHLOROPHENYL)-N'-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]UREA
• 3,4-DIBROMO-1,5-DIMETHYL-1H-PYRAZOLE
• N1-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]ACETAMIDE
• N1-[2-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ETHYL]-4-CHLOROBENZENE-1-SULFONAMIDE
• N1,N1-DIMETHYL-N'1-[2-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ETHYL]ETHANIMIDAMIDE
• N-(4-CHLOROPHENYL)-N'-[2-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ETHYL]THIOUREA
• N-METHYL-N'-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]UREA
• ETHYL 2-CYANO-3-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ANILINO]ACRYLATE
• N1-(4-CHLOROBENZYLIDENE)-4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)ANILINE
• N1-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]-4-CHLOROBENZENE-1-SULFONAMIDE
• N1-[4-(3,4,5-TRIBROMO-1H-PYRAZOL-1-YL)PHENYL]-4-CHLOROBENZAMIDE