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HRID 459755作成日:2026年10月26日

Triethylamine → 3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-one

https://huagongshe.com/reaction/459755

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Fluoro-3-nitrobenzaldehydeHCID 598129—
反応物Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624589—

反応手順

A stirred solution of dimethyl 3-oxo-1,3-dihydroisobenzofuran-1-ylphosphonate (20 g, 0.083 mol) and 4-fluoro-3-nitrobenzaldehyde (13.97 g, 0.083 mol) in tetrahydrofuran (120 ml) was cooled to 15° C. and triethylamine (11.5 ml, 0.083 mol) was added dropwise at <25° C. The mixture thickened at this point, so further tetrahydrofuran (50 ml) was added to aid stirring. The mixture was stirred at ambient temperature for 65 hours and the resulting solid was collected by filtration. The filtrate was concentrated in vacuo, the residue was triturated with water (30 ml) and the resulting solid was collected by filtration. The two crops of solid were combined and suspended in water (120 ml). The mixture was stirred at ambient temperature for 30 minutes and the resulting solid was collected by filtration and dried in vacuo for 24 hours to give crude 3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-one, still slightly wet with water, which was used directly in the next stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196085B2
出典データセットuspto-grants-2007_03
ORD IDord-3b69a254da05497aae7b0e857a4bf4d4
出典メモuspto-grants-2007_03