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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696680Erstellt: 26. Oktober 2026

5-Nitrofurfural → HCID 178519733, Verbindung

https://huagongshe.com/reaction/1696680

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-NitrofurfuralHCID 12774—
EduktSodium hydrideHCID 24758—
EduktHCID 178506355HCID 178506355—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178519733HCID 17851973362,3%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163768B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-15a61c4e45b94032b954eb665463ae8f
Quellennotizuspto-grants-2012_04