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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241268Generated: October 26, 2026

Acetic Acid → 1-((4-Bromofuran-2-yl)methyl)-4-methylpiperazine

https://huagongshe.com/reaction/2241268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant1-MethylpiperazineHCID 53167—
Reactant4-Bromo-2-furaldehydeHCID 2757010—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-((4-Bromofuran-2-yl)methyl)-4-methylpiperazineHCID 16099180—

Reaction Steps

To a stirred mixture of 4-bromofuran-2-carbaldehyde (2.10 g, 12.0 mmol) and THF (10 mL) that was cooled in an ice bath was added 1-methylpiperazine (1.60 ml, 14.4 mmol) dropwise, followed by sodium triacetoxyborohydride (3.81 g, 18.0 mmol) in 3 portions as solid. Acetic acid (0.343 ml, 6.00 mmol) was added, and the reaction was stirred for 18 hours at ambient temperature. The dark mixture was diluted with water (10 mL) and basified to pH>12 by addition of 5N NaOH. The mixture was extracted with diethyl ether (3×50 mL). The combined organic phases were dried (Na2SO4), filtered, and concentrated in vacuo. The resulting black oil (2.10 g, 66%) was carried forward without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723330B2
Source datasetuspto-grants-2010_05
ORD IDord-569affb3dc5d46d68f3789f3aab2719a
Source noteuspto-grants-2010_05