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HRID 991323作成日:2026年10月27日

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/reaction/991323

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物3-BromofuranHCID 89164—
反応物3-Formylphenylboronic acidHCID 2734356—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(Furan-3-yl)benzaldehydeHCID 2350601010%

反応手順

EX-601A) To a toluene (10 mL) solution of 3-bromofuran (0.54 mL, 6.0 mmol) was added 3-formylphenylboronic acid (1.00 g, 6.7 mmol) and DMF (4 mL). To the resulting solution was added K2CO3 (1.85 g, 13.4 mmol) and Pd(PPh3)4 (0.40 g, 0.35 mmol). The slurry was heated to reflux under argon for 2 h. The cooled mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.10 g (10%) of the desired 3-(3-furanyl)benzaldehyde product as a yellow oil. MS: m/Z=173.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462092B1
出典データセットuspto-grants-2002_10
ORD IDord-58e0644d67e643759d051af0bbe12188
出典メモuspto-grants-2002_10