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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-(1-Methylpropylidene)hydrazinecarboxamideHCID 12213—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Product3-Ethyl-1H-pyrazole-4-carbaldehydeHCID 17843803716%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318762B2
Source datasetuspto-grants-2012_11
ORD IDord-f5c4103b72f2409d939854df2da2879e
Source noteuspto-grants-2012_11