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HRID 1696680作成日:2026年10月27日

5-Nitrofurfural → HCID 178519733、化合物

https://huagongshe.com/reaction/1696680

反応式

関与物質

役割名称HCID仕込み量
反応物5-NitrofurfuralHCID 12774—
反応物Sodium hydrideHCID 24758—
反応物HCID 178506355HCID 178506355—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178519733HCID 17851973362.3%

反応手順

A solution of 2-mercapto-5-trifluoromethoxy-benzimidazole (1.26 g, 5.38 mmol) in tetrahydrofuran (10 ml) is added dropwise to a mixture of sodium hydride (60% dispersion in mineral oil, 0.344 g, 8.61 mmol) and tetrahydrofuran (5 ml) at 0° C. The mixture is stirred at room temperature for 2 hours. A solution of 5-nitro-2-furaldehyde (0.76 g, 5.38 mmol) in tetrahydrofuran (15 ml) is then added dropwise over a 15 minute period and the mixture is stirred for 16 hours at room temperature. The reaction mixture is concentrated under reduced pressure and the residue is dissolved in 10 ml of dichloromethane and filtered through a silica gel plug (40 ml). The silica gel plug is eluted with 800 ml of cylohexane/ethyl acetate (7/3, v/v). The organic filtrates are combined and concentrated under reduced pressure to yield 1.1 g of 5-(5-trifluoromethoxy-1H-benzoimidazol-2-ylsulfanyl)-furan-2-carbaldehyde as an oil. Yield=62%. Analytical LC/MS (method B): retention time=3.77 min., m/z=329.0 (positive ion mode).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163768B2
出典データセットuspto-grants-2012_04
ORD IDord-15a61c4e45b94032b954eb665463ae8f
出典メモuspto-grants-2012_04