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HRID 2105557作成日:2026年10月27日

Benzyl diethyl phosphate → 4-Benzyl-furan-2-carbaldehyde

https://huagongshe.com/reaction/2105557

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl diethyl phosphateHCID 298808—
反応物4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehydeHCID 3547541—
反応物5-Benzylfuran-2-carbaldehydeHCID 12418537—
触媒palladium(II) acetateHCID 167845—
溶媒Acetonitrile 2-propanolHCID 21921005—
生成物4-Benzyl-furan-2-carbaldehydeHCID 5964858541%

反応手順

The title compound was synthesized from 5-formylfuran-3-boronic acid pinacol ester (878 mg, 3.95 mmol), and benzyl diethyl phosphate (1.25 g, 5.14 mmol) using the same conditions used to synthesize 5-benzyl-furan-2-carbaldehyde, with the exception that TPP and Pd(OAc)2 were dissolved in 2:1 CH3CN/isopropyl alcohol. Purification by flash chromatography yielded 4-benzyl-furan-2-carbaldehyde as a white solid (300 mg, 41%). 1H NMR (400 MHz, CDCl3) δ ppm 9.56 (s, 1 H) 7.29-7.38 (m, 3 H) 7.24-7.28 (m, 2 H) 7.17 (d, J=3.5 Hz, 1 H) 6.19 (d, J=3.6 Hz, 1 H) 4.07 (s, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07579370B2
出典データセットuspto-grants-2009_08
ORD IDord-38e9e691354f4cd9a9ea970ac403aada
出典メモuspto-grants-2009_08