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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33467Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-NitrofurfuralHCID 12774—
Edukt2-(Piperidin-1-yl)anilineHCID 458795—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amineHCID 86595722—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429603B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-f1581ed5899248c99cc9d8b5f38f94e0
Quellennotizuspto-grants-2008_09