HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-Chloro-6-(2-methylphenoxy)-3-pyridazinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 23013971 | HCID 23013971 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloro-6-(2-methylphenoxy)-3-pyridazinol | HCID 178424395 | 85.9% |
Reaction Steps
A mixture comprising 578 mg (2.27 mmol) of 4,6-dichloro-3-(2-methylphenoxy)pyridazine obtained in Example 1 (2), acetic acid (10 mL) and 0.45 g (4.6 mmol) of potassium acetate was refluxed for 5 hours. The reaction mixture was allowed to stand for cooling, and after adding 50 mL of water, the mixture was extracted with ethyl acetate. The organic layers were combined, and washed successively with water and brine. After drying over anhydrous sodium sulfate, the solvent was removed to obtain 461 mg (1.95 mmol, Yield: 85.9%) of 5-chloro-6-(2-methylphenoxy)-3-pyridazinol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608563B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-a06722ce6e724bbab1669621691045c8 |
| Source note | uspto-grants-2009_10 |