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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579264Generated: October 30, 2026

Phenol → HCID 66695552, compound

https://huagongshe.com/reaction/579264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTolueneHCID 1140—
ReactantSodium hydrideHCID 24758—
Reactant4-(2,6-Diethyl-4-methylphenyl)-2,6-dimethyl-5-methylsulfonyl-2,3-dihydro-3-pyridazinoneHCID 56942717—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 66695552HCID 6669555229.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040709B2
Source datasetuspto-grants-2015_05
ORD IDord-6ce053ce01f44055bb13f426bcb44f4e
Source noteuspto-grants-2015_05