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HRID 422549作成日:2026年10月25日

Tetrahydrofuran → Ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoate

https://huagongshe.com/reaction/422549

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Ethyl 3-(1-chlorophthalazin-6-yl)-4-methylbenzoateHCID 59726010—
反応物HCID 178418573HCID 178418573—
触媒Ferric acetylacetonateHCID 5483663—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoateHCID 59726018—

反応手順

A 150-ml round-bottom flask under argon was charged with ethyl 3-(1-chlorophthalazin-6-yl)-4-methylbenzoate (358 mg, 1096 μmol), iron(III) acetylacetonate (38.7 mg, 109.6 □mol), THF (4200 μl), and 1-methyl-2-pyrrolidinone (420 μl). Methylmagnesium bromide (1.4M solution in toluene/tetrahydrofuran (75:25); 1174 μl, 1643 μmol) was then added via a syringe to the resulting orange red suspension, causing an immediate color change to brown, and finally to violet. The resulting mixture was stirred for 10 min, and the reaction (which remained a suspension) was diluted with EtOAc and carefully quenched with a few drops of 10% aqueous HCl solution. The mixture was washed with saturated aqueous NaHCO3 solution and the organic layer was dried (MgSO4), filtered, and concentrated in vacuo. CombiFlash purification (20% to 90% EtOAc in Hexanes) afforded ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoate as a light golden brown oil. MS (ES+): 307.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101612B2
出典データセットuspto-grants-2012_01
ORD IDord-e452b98d6b1042638a46b3596af5928a
出典メモuspto-grants-2012_01