戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 990418作成日:2026年10月25日

1,4-Dioxane → Ketone, 3-furyl phenyl

https://huagongshe.com/reaction/990418

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物3-BromobenzaldehydeHCID 76583—
反応物Potassium FluorideHCID 522689—
反応物2-(Tributylstannyl)furanHCID 4393688—
触媒HCID 178418476HCID 178418476—
溶媒Ethyl AcetateHCID 8857—
生成物Ketone, 3-furyl phenylHCID 20164086%

反応手順

EX-592A) To a dioxane (20 mL) solution of 3-bromobenzaldehyde (0.63 mL, 5.4 mmol) was added 2-(tributylstannyl)furan (1.89 ml, 6.00 mL) and Pd(PPh3)2Cl2 (0.21 g, 0.30 mmol). The mixture was heated to reflux under argon for 1.5 h. The cooled mixture was poured into a mixture of saturated KF and ethyl acetate and stirred 18 h. The slurry was filtered through celite. The organic layer was separated, 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 0.80 g (86%) of the desired 3-(2-furanyl)benzaldehyde product as an yellow oil which solidified upon standing. MS: m/z=173.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06458803B1
出典データセットuspto-grants-2002_10
ORD IDord-b2b3f0360fd34d9594dfe1154a35c509
出典メモuspto-grants-2002_10