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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711212Generated: October 27, 2026

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

https://huagongshe.com/reaction/1711212

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), 6.4 (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 numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-013e2fe47eb843389014edee83f4de5b
Source noteuspto-grants-2010_09