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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042600생성일: 2026년 10월 25일

3,4,5-Trimethoxybenzaldehyde → 3-(2-Furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-one

https://huagongshe.com/reaction/1042600

반응식

참여 물질

역할이름HCID투입량
반응물3,4,5-TrimethoxybenzaldehydeHCID 6858—
반응물Furan, 2-ethynyl-HCID 140409—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(2-Furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-oneHCID 57421963—

반응 조건

온도-78 °C

반응 단계

2-Ethynylfuran (200 mg, 2.17 mmol) was dissolved in dry THF (10 ml) and cooled to −78° C. under N2 atmosphere. BuLi (1.2 ml, 2.4 mmol) was added slowly and stirred at −78° C. for 10 min and then 3,4,5-trimethoxybenzaldehyde (500 mg, 2.6 mmol) was added and reaction mixture was stirred for 1 h at −78° C. and then reaction temp raised to room temp. The reaction was quenched by addition of aqueous NH4Cl solution and extracted with EtOAc. The colorless oil was dissolved in dichloromethane and excess of MnO2 was added to it and stirred overnight at room temp. The reaction mixture was filtered through celite plug and evaporated to dryness. 3-(2-furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-one was precipitated from ether by slow addition of hexane as off-white powder (65%). 1H NMR (300 MHz, CDCl3) δ 3.93 (s, 9H), 6.50-6.52 (m, 1H), 7.01 (d, J=3.6 Hz, 1H), 7.45 (s, 2H), 7.24 (s, 1H), 7.55 (d, J=1.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557982B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-077b0e23ea9b4bdd83fed3acfe65f9a4
출처 메모uspto-grants-2013_10