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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367811Generated: November 3, 2026

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

https://huagongshe.com/reaction/2367811

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 numberUS08697716B2
Source datasetuspto-grants-2014_04
ORD IDord-5290c2d5677b48b1b463251bda470328
Source noteuspto-grants-2014_04