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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633404Generated: October 27, 2026

Potassium Carbonate → 5-Nitro-2-(4-(oxetan-3-yl)piperazin-1-yl)benzonitrile

https://huagongshe.com/reaction/633404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-nitrobenzonitrileHCID 519417—
Reactant1-(Oxetan-3-yl)piperazineHCID 57416287—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Nitro-2-(4-(oxetan-3-yl)piperazin-1-yl)benzonitrileHCID 8670450197%

Reaction Steps

A mixture of 2-fluoro-5-nitrobenzonitrile (7 g, 1.2 eq, 41.2 mmol), 1-(oxetan-3-yl)piperazine (5.0 g, 1.0 eq, 35.2 mmol) was dissolved in annhydrous DMF (100 mL). K2CO3 (12.2 g, 2.5 eq, 87.9 mmol) was added to the above solution and the reaction mixture was stirred at room temperature for over night. The reaction mixture was diluted with of EtOAc (100 mL) and partitioned with H2O (100 mL). Layers were separated and the aqueous layer was washed once with of EtOAc (100 mL). Combined organic layers were dried over Na2SO4 and concentrated under reduced pressure to leave a crude oil. Purification of the crude mixture by column chromatography on silica gel (ISCO System) using 20% MeOH in CH2Cl2/CH2Cl2 (gradient system from 1:9 to 4:6) as eluent gave 5-nitro-2-(4-(oxetan-3-yl)piperazin-1-yl)benzonitrile in 97% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-fdb6ae427b0b40d0a5f853ab44ce86a7
Source noteuspto-grants-2016_04