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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409347Generated: October 25, 2026

Diethyl Oxalate → ethyl 1'H,2H-[3,3'-bipyrazole]-5-carboxylate

https://huagongshe.com/reaction/1409347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazinium chlorideHCID 115031—
Reactant1-(1H-pyrazol-3-yl)ethan-1-oneHCID 333471—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productethyl 1'H,2H-[3,3'-bipyrazole]-5-carboxylateHCID 7098123822.8%

Reaction Conditions

Temperature75 °C

Reaction Steps

Pieces of sodium (0.26 g) were slowly added to ethanol (12 ml) with stirring until all sodium had dissolved. 1-(1H-Pyrazol-5-yl)ethanone (8.61 mmol, 0.948 g) and diethyl oxalate (8.61 mmol, 1.258 g) was added. The mixture was heated to 75° C. for 3 h after which the stirring continued at RT overnight. Hydrazine hydrochloride (8.61 mmol, 0.590 g) dissolved in water (6 ml) was added. The resulting mixture was again heated to 75° C. for 3 h. The mixture was cooled to RT and neutralized by adding 2 M NaOH. The mixture was extracted twice with EtOAc and the combined organics were washed with water and brine. The organic phase was dried, filtered and evaporated. The crude product was purified by flash chromatography. 0.404 g of the title compound was obtained. 1H-NMR (400 MHz, MeOH-d4): δ 1.39 (t, 3H), 4.38 (q, 2H), 6.69 (d, 1H), 7.10 (bs, 1H), 7.70 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921378B2
Source datasetuspto-grants-2014_12
ORD IDord-9bb17615e04145528bfd3b139301a72d
Source noteuspto-grants-2014_12