HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57091Generated: October 26, 2026
Ethyl Acetate → 3-(3-chloro-1H-pyrazol-1-yl)pyridine
https://huagongshe.com/reaction/57091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Chloro-1-(pyridine-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride | HCID 118021782 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | 3-(3-chloro-1H-pyrazol-1-yl)pyridine | HCID 67499540 | 73.4% |
Reaction Steps
3-Chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride (1.00 g, 3.65 mmol) was stirred in N,N-dimethylformamide (10 mL). Copper(II) oxide (58.0 mg, 0.730 mmol) was added and the reaction was heated at 120° C. for 16 hours, at which point the reaction was ˜20% complete. Additional copper(II) oxide (112 mg, 1.46 mmol) was added and the reaction was stirred for 5 hours, at which point the reaction was complete by thin layer chromatography (TLC) [Eluent: ethyl acetate]. The mixture was diluted with ammonium hydroxide (NH4OH) and water and extracted with ethyl acetate. The organic layer was washed with 15% lithium chloride and concentrated to provide an orange solid. The residue was purified by flash column chromatography using ethyl acetate as eluent and the pure fractions were concentrated to afford the desired product as a white solid (481 mg, 69.7%). The spectral characterization was in agreement with the product prepared previously.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434712B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-e057a9d09fff4e41a0af34e569f9968e |
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| Source note | uspto-grants-2016_09 |
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