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HRID 1174600作成日:2026年10月25日

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

https://huagongshe.com/reaction/1174600

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-DihydrofuranHCID 70934—
反応物5-Iodo-1,2,3-trimethoxybenzeneHCID 298133—
反応物Potassium AcetateHCID 517044—
触媒TriphenylphosphineHCID 11776—
触媒Tetrabutylammonium ChlorideHCID 70681—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3,4,5-Trimethoxyphenyl)-2,3-dihydrofuranHCID 2247895243.1%

反応条件

温度80 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07838520B2
出典データセットuspto-grants-2010_11
ORD IDord-875e2d86da8e4d2d97d66fd45277102b
出典メモuspto-grants-2010_11