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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577185Generated: October 28, 2026

4-chloro-1-methyl-1H-pyrazole-3-carbaldehyde → (4-chloro-1-methyl-1H-pyrazol-3-yl)methanol

https://huagongshe.com/reaction/577185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-1-methyl-1H-pyrazole-3-carbaldehydeHCID 2782153—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(4-chloro-1-methyl-1H-pyrazol-3-yl)methanolHCID 5525517190%

Reaction Steps

To a solution of 4-chloro-1-methyl-1H-pyrazole-3-carbaldehyde (10.0 g, 69.2 mmol) in methanol (190 mL) was added sodium borohydride (3.93 g, 104 mmol) at 0° C. The mixture was stirred for 2 hours at room temperature and quenched with water. The solvent was evaporated, water was added, and the mixture was extracted 3 times with ethyl acetate. The combined organic phase was washed with brine and dried over sodium sulfate. After evaporation of the solvent, (4-chloro-1-methyl-1H-pyrazol-3-yl)methanol was obtained (9.04 g, 90% yield) and used in the next step without further purification; 1H NMR (500 MHz, DMSO-d6): δ 3.77 (s, 3H), 4.35 (d, J=5.5 Hz, 2H), 5.03 (t, J=5.5 Hz, 1H), 7.84 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-894f08e5df134d73b02bc8c178bb31c7
Source noteuspto-grants-2015_05