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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714660Generated: November 2, 2026

N-bromobutanimide → 1-[4-(4-Amino-3-bromo-phenyl)-piperidin-1-yl]-ethanone

https://huagongshe.com/reaction/1714660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-[4-(4-Aminophenyl)piperidin-1-yl]ethanoneHCID 59128551—
SolventDichloromethaneHCID 6344—
Product1-[4-(4-Amino-3-bromo-phenyl)-piperidin-1-yl]-ethanoneHCID 59128592—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1-[4-(4-amino-phenyl)-piperidin-1-yl]-ethanone (as prepared in the previous step, 0.36 g, 1.66 mmol) in CH2Cl2 (10 mL) was cooled to −78° C. and treated with NBS (0.28 g, 1.58 mmol) as a suspension in CH2Cl2 (4 mL). The reaction was allowed to warm to room temperature and stir for 30 min. The reaction was diluted with CH2Cl2 and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo. The crude material was used directly in the next reaction. LC-MS (ESI, m/z): Calcd. for C13H17BrN2O 297.1 (M+H), found 297.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795279B2
Source datasetuspto-grants-2010_09
ORD IDord-85d9ffd1aeba46df953a5a5c18a11808
Source noteuspto-grants-2010_09