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HRID 54975作成日:2026年10月25日

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

https://huagongshe.com/reaction/54975

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物2-Benzoylbenzoic AcidHCID 6813—
反応物2-HydrazinoethanolHCID 8017—
反応物Sodium hydrideHCID 24758—
反応物Hydroxyethyl-phthalazinoneHCID 14322325—
反応物HCID 178418361HCID 178418361—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-Methoxyethyl)-4-phenyl-1(2H)-phthalazinoneHCID 1995707147%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624922
出典データセットuspto-grants-1997_04
ORD IDord-21297e0e110f42bc94fefd9751f49c00
出典メモuspto-grants-1997_04