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4-bromo-3-(bromomethyl)-1-methyl-1H-pyrazole synthesis

3synthesis methods
5775-82-6 Synthesis
AKOS B019512

5775-82-6
88 suppliers
$10.00/250mg

4-bromo-3-(bromomethyl)-1-methyl-1H-pyrazole

1383575-45-8
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Yield:1383575-45-8 465 mg

Reaction Conditions:

with N-Bromosuccinimide;azobisisobutyronitrile in chlorobenzene at 80; for 7 h;

Steps:

0142-1 0142-1

0142-1
2,2'-Azobis(isobutyronitrile) (27 mg) was added to a solution of 4-bromo-1,3-dimethyl-1H-pyrazole (286 mg) and N-bromosuccinimide (320 mg) in chlorobenzene (6 mL), followed by stirring at 80° C. for 7 hours.
The reaction mixture was cooled to room temperature, and ethyl acetate and a saturated sodium hydrogen carbonate aqueous solution were added thereto.
The organic layer was collected by separation, washed with a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure, thereby obtaining 4-bromo-3-(bromomethyl)-1-methyl-1H-pyrazole (465 mg) as a white solid.
MS m/z (M+H): 253.

References:

US2015/322063,2015,A1 Location in patent:Paragraph 0970; 0971; 0972

915707-65-2 Synthesis
(4-Bromo-1-methyl-1H-pyrazol-3-yl)methanol

915707-65-2
57 suppliers
$44.00/250mg

4-bromo-3-(bromomethyl)-1-methyl-1H-pyrazole

1383575-45-8
3 suppliers
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211738-66-8 Synthesis
4-BROMO-1-METHYL-1 H-PYRAZOLE-3-CARBOXYLIC ACID M ETHYL ESTER

211738-66-8
98 suppliers
$35.00/100mg

4-bromo-3-(bromomethyl)-1-methyl-1H-pyrazole

1383575-45-8
3 suppliers
inquiry