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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447956Generated: October 30, 2026

N-bromobutanimide → 4-(4-Amino-3-bromo-phenyl)-piperidine-2,6-dione

https://huagongshe.com/reaction/447956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-Aminophenyl)piperidine-2,6-dioneHCID 59771154—
SolventDichloromethaneHCID 6344—
Product4-(4-Amino-3-bromo-phenyl)-piperidine-2,6-dioneHCID 5977127494%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 106 mg (0.519 mmol) of 4-(4-amino-phenyl)-piperidine-2,6-dione (as prepared in the previous step) in CH2Cl2 (20 mL) was cooled to 0° C. and treated with 92.4 mg (0.519 mmol) of NBS for 35 min. The mixture was diluted with CH2Cl2 (50 mL) and washed with saturated aqueous NaHCO3 (2×40 mL) and water (1×40 mL). The organic layer was dried (MgSO4) and concentrated in vacuo to afford 138 mg (94%) of the title compound as a tan solid: Mass spectrum (ESI, m/z): Calcd. for C11H11N2O2Br, 283.0/285.0 (M+H), found 283.1/285.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481564B2
Source datasetuspto-grants-2013_07
ORD IDord-52936a03cdcd466ba6eb4a24e523318c
Source noteuspto-grants-2013_07