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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde | HCID 703492 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Chlorophenyl)-1-phenyl-1H-pyrazole-4-methanol | HCID 740178 | 93.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04325962 |
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| Source dataset | uspto-grants-1982_04 |
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| ORD ID | ord-28e4665cb67a4ffa8f6de19327c68a75 |
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| Source note | uspto-grants-1982_04 |
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