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HRID 45627作成日:2026年10月25日

Hydrochloric Acid → 2-Fluorobenzofuran-5-carbaldehyde

https://huagongshe.com/reaction/45627

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IodineHCID 807—
反応物TetrahydrofuranHCID 8028—
反応物MagnesiumHCID 5462224—
反応物5-Bromo-2-fluoro-1-benzofuranHCID 57439113—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Fluorobenzofuran-5-carbaldehydeHCID 45090831—

反応手順

A slurry of magnesium powder (219 mg) and iodine (cat) in dry tetrahydrofuran (3 ml) was heated at 50° C. under nitrogen for 20 minutes. 5-Bromo-2-fluoro-1-benzofuran (1.4 g) was dissolved in dry tetrahydrofuran (6 ml). A 1 ml portion of the solution was added to the slurry at 50° C. without stirring. After 30 minutes the rest of the solution was added slowly and the reaction was heated at reflux for 3 hours. The reaction was cooled in an ice/water bath and dimethylformamide (1 ml) was added dropwise maintaining the temperature below 10° C. After 1 hour a mixture of 2N hydrochloric acid (12.5 ml) and brine (12.5 ml) was added. The reaction mixture was extracted using ethyl acetate (3×25 ml). The combined organics were washed with brine and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo and the residue applied to a silica cartridge (50 g). This was eluted with cyclohexane, cyclohexane/ethyl acetate (6:1, 5:1 v/v). This gave 2-fluoro-5-formyl-1-benzofuran (376 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541579B2
出典データセットuspto-grants-2013_09
ORD IDord-f85faedff01e4a4cbbd3deb2185f6973
出典メモuspto-grants-2013_09