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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910781Generated: November 2, 2026

Acetic Acid → HCID 51263596, compound

https://huagongshe.com/reaction/1910781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
ReactantSodium cyanoborohydrideHCID 5003444—
ProductHCID 51263596HCID 5126359654%

Reaction Steps

To a solution of 1-(4-nitrophenyl)-piperazine (0.6 g, 2.89 mmol) in THF (10 mL) was added fufaraldehyde (0.41 g, 4.31 mmol), acetic acid (3 mL) and water (1.5 mL) and the mixture stirred at r.t. for half an hour. Sodium cyanoborohydride (0.27 g, 4.31 mmol) was added and the reaction heated at reflux for four hours. The reaction was cooled and the solvent evaporated. The resulting residue was diluted with water and extracted with dichloromethane. The combined organic layers were washed with saturated sodium bicarbonate and brine solution, dried over sodium sulfate, filtered and concentrated. Purification by column chromatography over silica gel (60-120 mesh) using 5% methanol/chloroform as eluent afforded 1-furan-2-ylmethyl-4-(4-nitrophenyl)-piperazine (0.45 g, 54%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-dfd454b330d14f3799d0027c4b512596
Source noteuspto-grants-2013_12