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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54975Generated: October 25, 2026

Methyl iodide → 2-(2-Methoxyethyl)-4-phenyl-1(2H)-phthalazinone

https://huagongshe.com/reaction/54975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Benzoylbenzoic AcidHCID 6813—
Reactant2-HydrazinoethanolHCID 8017—
ReactantSodium hydrideHCID 24758—
ReactantHydroxyethyl-phthalazinoneHCID 14322325—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Methoxyethyl)-4-phenyl-1(2H)-phthalazinoneHCID 1995707147%

Reaction Steps

Eighty-five grams (0.38 mole) of 2-benzoylbenzoic acid and 28.6 g (0.38 mole) of hydroxyethylhydrazine were reacted according to the procedure of Example 185. The resulting hydroxyethyl-phthalazinone was suspended in 300 mL of DMF and 200 mL THF and 12.3 g of 60% sodium hydride in oil was added in portions over 40 minutes under nitrogen. The reaction was stirred an additional 45 minutes at room temperature and the evolution of hydrogen ceased. Thirty-one milliliters of methyl iodide was added over 1.5 hours and the reaction was stirred at gentle reflux for 16 hours. It was poured into water and extracted into ether. The ether layers were dried over sodium sulfate and stripped. The residue was chromatographed on silica with 5% ethylamine in ethyl acetate to provide 39 g (47%) of product, mp 115-118 after recrystallization from cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624922
Source datasetuspto-grants-1997_04
ORD IDord-21297e0e110f42bc94fefd9751f49c00
Source noteuspto-grants-1997_04