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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024076Generated: October 29, 2026

1-(4-Nitrophenyl)piperazine → 1-(4-Nitrophenyl)-4-(oxetan-3-yl)piperazine

https://huagongshe.com/reaction/1024076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-OxetanoneHCID 15024254—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Product1-(4-Nitrophenyl)-4-(oxetan-3-yl)piperazineHCID 8668415276.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 117c (2.0 g, 8.23 mmol), zinc chloride (2.2 g, 16.4 mmol), oxetan-3-one (1.18 g, 16.4 mmol) in methanol (80 mL) was added NaBH3CN (1.02 g, 16.4 mmol). The mixture was stirred at 50° C. for 5 hours. The mixture was then concentrated under reduced pressure and the residue was diluted with water (100 mL). It was extracted with dichloromethane (3×100 mL) and the combined organic layer was concentrated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 4:1 petroleum ether/ethyl acetate to afford 117d (1.65 g, 76%) as a yellow solid. MS: [M+H]+ 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722676B2
Source datasetuspto-grants-2014_05
ORD IDord-23338a47893f43129b7db68213723005
Source noteuspto-grants-2014_05