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HRID 459778作成日:2026年10月25日

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

https://huagongshe.com/reaction/459778

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-Methoxy-3-nitrobenzaldehydeHCID 700608—
反応物Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-methoxy-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624699—

反応条件

温度15 °C

反応手順

A stirred solution of dimethyl 3-oxo-1,3,-dihydroisobenzofuran-1-ylphosphonate (2.42 g, 0.01 mol; prepared in a manner similar to that described in Example 23) and 4-methoxy-3-nitrobenzaldehyde (1.81 g, 0.01 mol) in tetrahydrofuran (15 ml) was cooled to 15° C. and a solution of triethylamine (1.01 g, 0.01 mol) in tetrahydrofuran (1.5 ml) was added dropwise at <25° C. The mixture was stirred at ambient temperature for 4 hours, allowed to stand at this temperature for a further 16 hours and the resulting mixture was concentrated in vacuo. The residue was triturated with water (50 ml) and stirred at ambient temperature for 2 hours before the resulting solid was collected by filtration and dried in vacuo for 24 hours to give crude 3-(4-methoxy-3-nitrobenzylidene)-3H-isobenzofuran-1-one (2.53 g) as a yellow solid, m.pt. 173–181° C., 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-57d87a8d33454567be00b86794b82fc6
出典メモuspto-grants-2007_03