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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57558Generated: October 30, 2026

Hydrogen Bromide → 1-(4-Bromo-2-fluorophenyl)piperazine

https://huagongshe.com/reaction/57558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dimethylethyl 4-(4-amino-2-fluorophenyl)-1-piperazinecarboxylateHCID 16203630—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product1-(4-Bromo-2-fluorophenyl)piperazineHCID 3251309—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 4-(4-amino-2-fluorophenyl)piperazine-1-carboxylate (885 mg, 3 mmol) in 8 mL of aq HBr was added a solution of NaNO2 (228 mg, 3.3 mmol) in 2 mL of H2O at 0° C., then the mixture was stirred at 0° C. for 40 minutes. After that, the mixture was poured into a solution of CuBr (905 mg, 6.3 mmol) in 8 mL aq HBr at 0° C. The reaction was heated to 60° C. and stirred for 2 hours. After cooling, the mixture was based with 2M NaOH to pH=8-9 and extracted with EA, washed with H2O and brine, dried and concentrated to give black solid. MS (m/z): 261 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-4440b4b8e8754b9f8a5b54902b1bd457
Source noteuspto-grants-2016_09