HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323574Generated: October 30, 2026
Ethyl cyanoacetate → HCID 22006193, compound
https://huagongshe.com/reaction/323574
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 54095431 | HCID 54095431 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22006193 | HCID 22006193 | — |
Reaction Steps
An intimate, magnetically stirred mixture of 440 mg (1.40 mmol) of 1-[(4-methylphenyl)thio]-1-[(4-methoxyphenyl)hydrazono]-2-propanone 370 μl of ethylcyanoacetate and 178 mg of ammonium acetate was heated under a nitrogen atmosphere at 160° C. for 30 min. The reaction mixture was cooled and dissolved in methylene chloride. The organic layer was washed successively with saturated aqueous sodium bicarbonate and water. The organic layer was dried over magnesium sulfate and evaporated in vacuo to yield semi-pure product. The residue was recrystallized from ethanol to yield 6-[(4-methylphenyl)thio]-2,3-dihydro-2-(4-methoxyphenyl)-5-methyl-3-oxo-4-pyridazinecarbonitrile, mp 148-149° C.(EtOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214810B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-59922d7eea8e40d9a07d4d2c28c44496 |
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| Source note | uspto-grants-2001_04 |
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