Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 6-(Propan-2-yl)-4,5-dihydropyridazin-3(2H)-one | HCID 23028092 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Isopropyl-3-pyridazinone | HCID 23028147 | — |
Reaction Steps
4,5-Dihydro-6-isopropyl-3 (2H)-pyridazinone (3.10 g) was dissolved in acetic acid (30.0 ml), and bromine (3.50 g, 22.0 mmol) was added dropwise to the solution over 10 minutes under heating at 100° C. with stirring. After the reaction solution was heated for 1 hour under reflux, the acetic acid was distilled away under reduced pressure, and water (100 ml) was added to the residues which were then extracted 5 times with ethyl acetate. The extracts were combined, dried over anhydrous magnesium sulfate and concentrated to give a crude product of 6-isopropyl-3 (2H)-pyridazinone. The yield was 3.30 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816526B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-36e88ef656cd4951b6257773619e1d31 |
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| Source note | uspto-grants-2010_10 |
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