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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | 1-(1H-pyrazol-3-yl)ethan-1-one | HCID 333471 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 1'H,2H-[3,3'-bipyrazole]-5-carboxylate | HCID 70981238 | 22.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921378B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9bb17615e04145528bfd3b139301a72d |
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| Source note | uspto-grants-2014_12 |
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