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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33467생성일: 2026년 10월 24일

5-Nitrofurfural → 5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amine

https://huagongshe.com/ko/reaction/33467

반응식

참여 물질

역할이름HCID투입량
반응물5-NitrofurfuralHCID 12774—
반응물2-(Piperidin-1-yl)anilineHCID 458795—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
생성물5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amineHCID 86595722—

반응 단계

A solution of 2-piperidinoaniline (1 mmol), 5-nitro-furan-2-carbaldehyde (1.1 mmol) and sodium triacetoxyborohydride (“NaBH(OAc)3”) (2 mmol) in anhydrous DCM (10 mL) was stirred 16 h at room temperature. The mixture was then washed successively with water, dilute aqueous sodium hydroxide (“NaOH”), water and brine before being dried over MgSO4, filtered and concentrated under reduced pressure. Purification of the residual oil by flash silica gel chromatography yielded the product. MS: 301 (M+1). LC/MS purity: 100%. 1H NMR (CDCl3, 300 MHz): δ 7.25 (d, 1H), 7.15-6.95 (m, 2H), 6.75 (t, 1H), 6.55 (d, 1H), 5.4 (bs, 1H), 4.45 (s, 2H), 2.8 (bm, 4H), 1.8-1.5 (bm, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429603B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f1581ed5899248c99cc9d8b5f38f94e0
출처 메모uspto-grants-2008_09