Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromhydrol | HCID 166749 | — |
| Reactant | HCID 22506970 | HCID 22506970 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9942980 | HCID 9942980 | 61.2% |
Reaction Steps
A mixture of 6-(2-methoxy-benzenesulfonyl)-2H-pyridazin-3-one (100 mg) and aluminum tri-bromide (2 g) was prepared and heated at 100° C. for two hours. The reaction mixture was cooled and water (10 mL) was added. The mixture was then extracted with chloroform. The organic extract was washed with water (2×10 mL), dried over anhydrous sodium sulfate and evaporated. The resulting residue was triturated with isopropyl ether and the resulting solid was collected by filtration to afford the title compound (61%, 58 mg), 1HNMR (CDCl3, 300 MHz), δ 7.0 (m, 3H), 7.6 (m, 2H), 7.8 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872722B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5f6147d3822349919ca10b7c2db4a044 |
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| Source note | uspto-grants-2005_03 |
|---|