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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33467Generated: October 26, 2026

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

https://huagongshe.com/reaction/33467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitrofurfuralHCID 12774—
Reactant2-(Piperidin-1-yl)anilineHCID 458795—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amineHCID 86595722—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429603B2
Source datasetuspto-grants-2008_09
ORD IDord-f1581ed5899248c99cc9d8b5f38f94e0
Source noteuspto-grants-2008_09