돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1696680생성일: 2026년 10월 26일

5-Nitrofurfural → HCID 178519733, 화합물

https://huagongshe.com/reaction/1696680

반응식

참여 물질

역할이름HCID투입량
반응물5-NitrofurfuralHCID 12774—
반응물Sodium hydrideHCID 24758—
반응물HCID 178506355HCID 178506355—
용매TetrahydrofuranHCID 8028—
생성물HCID 178519733HCID 17851973362.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163768B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-15a61c4e45b94032b954eb665463ae8f
출처 메모uspto-grants-2012_04