HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500536Generated: October 30, 2026
Acetyl chloride → Ethyl 6-oxo-1,6-dihydropyridazine-4-carboxylate
https://huagongshe.com/reaction/500536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 6-Oxo-1,6-dihydropyridazine-4-carboxylic acid | HCID 12376265 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 6-oxo-1,6-dihydropyridazine-4-carboxylate | HCID 12376258 | — |
Reaction Steps
The title compound from Example 18.3 (1.0 g, 7.13 mmol) was added to a solution of ethanol (16 mL) and acetyl chloride (4 mL) and the resulting suspension was heated to 75° C. and stirred overnight. The reaction mixture was concentrated, diluted with water and extracted with dichloromethane. The organic phase was dried over sodium sulfate, filtered and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772235B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-3aa33dedd9b04de8a50ea781e5e0a20b |
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| Source note | uspto-grants-2010_08 |
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