HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880353Generated: October 29, 2026
Dimethylformamide → 3-Ethyl-1H-pyrazole-4-carbaldehyde
https://huagongshe.com/reaction/1880353
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-(1-Methylpropylidene)hydrazinecarboxamide | HCID 12213 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Product | 3-Ethyl-1H-pyrazole-4-carbaldehyde | HCID 178438037 | 16% |
Reaction Steps
To cool DMF (50 mL) at 0° C., POCl3 (30 mL) was added dropwise over 30 minutes, and maintained at 0° C. for 1 hour. To the mixture was added butan-2-one semicarbazone (10 g, 78 mmol) in portions at 70° C. and maintained at 70° C. for 4 hours. The mixture was poured into crushed ice (700 g), neutralized using 10% NaOH solution and extracted using ethyl acetate (3×100 mL). The combined organic layers were washed with water (2×80 mL), saturated aqueous NaCl (100 mL), dried over anhydrous Na2SO4 and concentrated to obtain a crude product, which was purified by column chromatography (60-120 mesh silica gel) using 3-5% methanol in chloroform as eluents to afford 3-ethyl-1H-pyrazole-4-carbaldehyde (1.5 g, 16%) as solid. 1H NMR (CDCl3) δ 9.95 (s, 1H), 8.0 (s, 1H), 3.0 (q, 2H), 1.35 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318762B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-f5c4103b72f2409d939854df2da2879e |
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| Source note | uspto-grants-2012_11 |
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