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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600268생성일: 2026년 10월 25일

Tetrahydrofuran → 3-(4-Nitro-thiophen-2-ylmethylene)-3H-isobenzofuran-1-one

https://huagongshe.com/reaction/600268

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물TriethylamineHCID 8471—
반응물4-Nitrothiophene-2-carbaldehydeHCID 818857—
반응물HCID 86628633HCID 86628633—
용매WaterHCID 962—
생성물3-(4-Nitro-thiophen-2-ylmethylene)-3H-isobenzofuran-1-oneHCID 68910119—

반응 단계

To a solution of (4-oxo-3,4-dihydro-phthalazin-1-yl)-phosphonic acid dimethyl ester (3.85 g, 15.9 mmol) in THF (30 mL) was added 4-nitro-thiophene-2-carbaldehyde (25) (2.5 g, 15.9 mmol) under nitrogen. Triethylamine (2.2 mL 15.9 mmol) was added dropwise over 10 minutes and then stirred at room temperature for 4 hours. The yellow suspension was poured in water (80 mL), and the then filtered, the solid was washed with water (15 mL), hexane (10 mL) and then diethyl ether (10 mL) and then dried in vacuo to afford a 4.1 g of the desired products. Two peaks in LC-MS analysis, (4.1 g, 94%) and required no further purification; m/z (LC-MS, ESP), RT=4.71 mins (M+H) 274, & RT=4.84 mins (M+H) 274;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902193B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-4d90028aa22a4d56ac086b9fbf7ce389
출처 메모uspto-grants-2011_03