HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076823Generated: October 31, 2026
Hydrochloric Acid → 3-Oxo-2,3-dihydropyridazine-4-carbonitrile
https://huagongshe.com/reaction/2076823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyanoacetic acid hydrazide | HCID 8820 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Oxo-2,3-dihydropyridazine-4-carbonitrile | HCID 12376256 | 21% |
Reaction Steps
To a mixture of glyoxal bis(sodium hydrogen sulfite) monohydrate (25.24 g, 88.8 mmol) in water (80 ml) was added slowly a solution of cyanoacetohydrazide (8 g, 80.7 mmol) in ethanol/water 2:1 (120 ml). The mixture was then heated to 40° C. for 30 min. The pH was adjusted to 12-13 by addition of 10 N NaOH and stirring was continued for 3 h at 40° C. and for 1 h at 60° C. The reaction mixture was then allowed to cool to ambient temperature over night. The pH was then adjusted to 1-2 by addition of conc. HCl and the resulting mixture was evaporated. The remaining solid was extracted with CHCl3 in a soxhlet-extractor for two days to obtain the title compound as a light brown solid (2.019 g, 16.67 mmol, 21%). 1H NMR (d6-DMSO): 8.07 (d, J=4 Hz, 1H), 8.12 (d, J=4 Hz, 1H), 13.91 (s br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928106B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-9c8a16fd0c244c1f805fee19ecca29d3 |
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| Source note | uspto-grants-2011_04 |
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