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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523107Generated: October 26, 2026

4-bromo-1-methyl-1H-pyrazole-5-carbaldehyde → (4-bromo-1-methyl-1H-pyrazol-5-yl)methanol

https://huagongshe.com/reaction/523107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-1-methyl-1H-pyrazole-5-carbaldehydeHCID 2794634—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(4-bromo-1-methyl-1H-pyrazol-5-yl)methanolHCID 5741577390%

Reaction Steps

To a solution of 4-bromo-1-methyl-1H-pyrazole-5-carbaldehyde (677 mg, 3.58 mmol) in MeOH (8 mL) at 0° C., NaBH4 (136 mg, 0.86 mmol) was added. The solution was stirred at room temperature for 2 hours. The reaction was concentrated in vacuo and diluted with water. The solution was extracted with EtOAc, the organic layer collected, dried over sodium sulphate and concentrated in vacuo to afford the title compound as a white solid (614 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334286B2
Source datasetuspto-grants-2016_05
ORD IDord-292f601f3fab4682ac53935aab33a93b
Source noteuspto-grants-2016_05