HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199126Generated: October 30, 2026
Potassium Hydroxide → HCID 59834464, compound
https://huagongshe.com/reaction/2199126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 59834519 | HCID 59834519 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59834464 | HCID 59834464 | 100% |
Reaction Steps
A solution of 2-[3,5-dibromo-4-(1-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-ethyl ester (40) (85 mg, 0.18 mmol) in methanol (0.5 mL) was treated with a 2N aqueous potassium hydroxide solution (90 μL, 0.18 mmol) at room temperature. The reaction mixture was heated to 55° C., stirred for 1 h and then was concentrated under reduced pressure. The resulting residue was diluted with methylene chloride (5 mL) and was washed with water (2×3 mL). The aqueous layers were re-extracted with methylene chloride (5 mL). The organic layers were combined and dried with sodium sulfate, filtered, and concentrated. The resulting solid was dried under high vacuum to afford 6-[2,6-dibromo-4-(2-hydroxy-ethyl)-phenoxy]-2-isopropyl-pyridazin-3-one (41) (77 mg, 100%) as a white solid that was used without further purification; LRMS for C15H16Br2N2O3 (M+CH3CN+H) m/z=474. Molecular Weight=432.1144; Exact Mass=429.9528
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE046024E1 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-a69be1b4fa244913a85ee103816ce549 |
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| Source note | uspto-grants-2016_06 |
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