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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252771생성일: 2026년 10월 26일

2,3-Dihydrofuran → 2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuran

https://huagongshe.com/reaction/252771

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DihydrofuranHCID 70934—
반응물5-Iodo-1,2,3-trimethoxybenzeneHCID 298133—
반응물Potassium AcetateHCID 517044—
촉매TriphenylphosphineHCID 11776—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuranHCID 2247895243.1%

반응 조건

온도80 °C

반응 단계

To a solution of 5-iodo-1,2,3-trimethoxybenzene (900 mg, 3.06 mmol) and 2,3-dihydrofuran (1.16 mL, 15.3 mmol) in dry DMF (8 mL) were added PPh3 (20 mg, 0.077 mmol), KOAc (901 mg, 9.18 mmol), n-Bu4NCl (850 mg, 3.06 mmol) and Pd(OAc)2 (17 mg, 0.077 mmol). The reaction mixture was stirred 18 h at 80° C. The reaction mixture was diluted with AcOEt and water. After separation, the organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude residue was then purified by flash chromatography on silica gel (AcOEt/Hexane: 20/80) to afford the title compound 287 (311 mg, 1.32 mmol, 43% yield). 1H NMR: (300 MHz, CDCl3) δ (ppm): 6.59 (s, 2H), 6.45 (m, 1H), 5.45 (dd, J=10.5, 8.4 Hz, 1H), 4.97 (m, 1H), 3.87 (s, 6H), 3.84 (s, 3H), 3.06 (m, 1H), 2.62 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868204B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a67bdf6bf52946058e0828fd58bfd8d7
출처 메모uspto-grants-2011_01