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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459755생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/459755

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-nitrobenzaldehydeHCID 598129—
반응물Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—
용매TetrahydrofuranHCID 8028—
생성물3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-oneHCID 68624589—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196085B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-3b69a254da05497aae7b0e857a4bf4d4
출처 메모uspto-grants-2007_03