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HRID 10747作成日:2026年10月26日

Cesium carbonate → 3-(Dihydro-2-furanyl)benzaldehyde

https://huagongshe.com/reaction/10747

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2,3-DihydrofuranHCID 70934—
反応物3-BromobenzaldehydeHCID 76583—
触媒HCID 178418851HCID 178418851—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物3-(Dihydro-2-furanyl)benzaldehydeHCID 2198109040%

反応条件

温度45 °C

反応手順

Ex-119A: 5-Bromobenzaldehyde (0.5 g, 2.7 mmol) and 2,3-dihydrofuran (0.56 g, 8.1 mmol) were dissolved in dioxane (5.0 mL). Nitrogen was bubbled into the solution for 15 min followed by the sequential addition of cesium carbonate (0.96 g, 2.9 mmol) and bis(tri-t-butylphosphine)palladium(0) (0.014 g, 0.027 mmol). The solution was immediately heated to 45° C. and aged for 24 h. Upon completion, as determined by HPLC, the reaction was diluted with water (20 mL) and extracted with ethyl acetate (3×20 mL). The combined organic extracts were dried over sodium sulfate and concentrated to a brown oil. Silica gel chromatography (ethyl acetate/hexanes, 1:9) gave 0.18 g (40%) of 3-(2,3-dihydro-furan-2-yl)-benzaldehyde as a clear, colorless oil. 1H-NMR (300 MHz, CDCl3) δ 10.03 (s, 1H), 7.88 (s, 1H), 7.82 (d, 1H, J=7.2 Hz), 7.62–7.64 (m, 1H), 7.53 (t, 1H, J=7.2 Hz), 6.48 (q, 1H, J=Hz), 5.60 (dd, 1H, J=8.1, 10.8 Hz), 4.98 (q, 1H, J=3.3 Hz), 3.15 (ddt, 1H, J=15.0, 8.1, 2.5 Hz), 2.59 (ddt, 1H, J=15.0, 8.1, 2.5 Hz). MS (EI) m/z=174 ([M]+, 100%). HRMS (EI) Calcd. for C11H10O2: 174.0681. Found: 174.0677.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094801B2
出典データセットuspto-grants-2006_08
ORD IDord-102420b016204a699014c908bf046c20
出典メモuspto-grants-2006_08