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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425971Generated: October 30, 2026

2,4-Difluoronitrobenzene → tert-Butyl 4-(5-Fluoro-2-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2425971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluoronitrobenzeneHCID 67967—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(5-Fluoro-2-nitrophenyl)piperazine-1-carboxylateHCID 22272537—

Reaction Steps

2,4-Difluoronitrobenzene (10.0 g, 62.9 mmol), t-butyl piperazine-1-carboxylate (11.7 g, 62.9 mmol) and N,N-diisopropylethylamine (8.10 g, 62.9 mmol) were stirred at room temperature in dry acetonitrile (100 mL) for 16 h. The solvent was removed by rotary evaporation and the residue was dissolved in dichloromethane and washed with water. The dichloromethane was removed by rotary evaporation to collect the title compound (19.0 g, 93%). 1H NMR (400 MHz, CDCl3): δ 7.91 (dd, 1H), 6.75 (m, 2H), 3.60 (m, 4H), 3.03 (m, 4H), 1.48 (s, 9H); MS (ESI) m/z: Calculated for C15H20FN3O4: 325.14; Observed: 348.1 (M++Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968538B2
Source datasetuspto-grants-2011_06
ORD IDord-bc696190c725432ab4dcb3c1a893b007
Source noteuspto-grants-2011_06