Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(2,6-Diethyl-4-methylphenyl)-2,6-dimethyl-5-methylsulfonyl-2,3-dihydro-3-pyridazinone | HCID 56942717 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66695552 | HCID 66695552 | 29.3% |
Reaction Steps
To a test tube (outside diameter: 21 mm Φ×overall length: 160 mm), phenol (108 mg), toluene (930 mg), and 60% of oily sodium hydride (44 mg) were added, and stirred at room temperature for 5 minutes. To the mixture, (4-(2,6-diethyl-4-methylphenyl)-2,6-dimethyl-5-methylsulfonyl-2,3-dihydropyridazin-3-one ((2-34)-(1)-39) (299 mg) was added, and stirred at room temperature for 1.5 hours and at 100° C. for 1.5 hours. To the mixture, benzyltriethylammonium chloride was added and stirred for 1.5 hours, and then DMSO (1.1 ml) was added and stirred for 2 hours. After the mixture was cooled to room temperature, water was added and extracted with toluene 3 times. The organic layers were combined, washed with 2N aqueous sodium hydroxide solution 3 times, and concentrated under reduced pressure. The residue was subjected to column chromatography (hexane: ethyl acetate=3:1) to give 91 mg of 4-(2,6-diethyl-4-methylphenyl)-2,6-dimethyl-5-phenoxy-2,3-dihydro-3-pyridazinone ((1-31)-(1)-39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040709B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-6ce053ce01f44055bb13f426bcb44f4e |
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| Source note | uspto-grants-2015_05 |
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