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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285978Generated: October 26, 2026

3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde → 3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-methanol

https://huagongshe.com/reaction/2285978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 703492—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-methanolHCID 74017893.1%

Reaction Steps

80 grams 1-phenyl-3-(p-chlorophenyl)-pyrazol-4-aldehyde were dissolved in a mixture of 800 milliliters ethanol and 1200 milliliters dimethylformamide. To the solution thus obtained, 5.5 grams 95% sodium borohydride were added in small portions at 20°-25° C. The mixture was then stirred for one more hour at room temperature. Thereafter, the reaction mixture was evaporated and the residue was taken up, with rubbing, with ethanol and water were thereafter added. The precipitate formed thereby was separated, dispersed and stirred in warm water, the precipitate was filtered off by suction, dried and recrystallized from benzene. 75 grams 4-hydroxymethyl-1-phenyl-3-(p-chloropheny)-pyrazol, melting at 141°-142° C., were obtained, representing a yield of 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04325962
Source datasetuspto-grants-1982_04
ORD IDord-28e4665cb67a4ffa8f6de19327c68a75
Source noteuspto-grants-1982_04