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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008917Generated: October 28, 2026

N-bromobutanimide → 4-(4-Amino-3-bromo-phenyl)-1-methyl-piperidine-2,6-dione

https://huagongshe.com/reaction/1008917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-Amino-phenyl)-1-methyl-piperidine-2,6-dioneHCID 59771129—
SolventDichloromethaneHCID 6344—
Product4-(4-Amino-3-bromo-phenyl)-1-methyl-piperidine-2,6-dioneHCID 5977121967%

Reaction Steps

A solution of 289 mg (1.32 mmol) of 4-(4-amino-phenyl)-1-methyl-piperidine-2,6-dione (as prepared in the previous step) in CH2Cl2 (15 mL) was treated portionwise with 224 mg (1.29 mmol) of solid NBS for 20 min. The mixture was diluted with CH2Cl2 (30 mL) and washed with saturated aqueous NaHCO3 (2×30 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. Silica gel chromatography of the residue with 25-50% EtOAc-hexane afforded 265 mg (67%) of the title compound as a tan solid: Mass spectrum (ESI, m/z): Calcd. for C12H13N2O2Br, 297.0/299.0 (M+H), found 297.0/299.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973035B2
Source datasetuspto-grants-2011_07
ORD IDord-ada8d1be29fd44b5990d5661f9bf2fd4
Source noteuspto-grants-2011_07