Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508092Generated: October 25, 2026

N-bromobutanimide → 2-Bromo-4-(2-morpholin-4-yl-ethyl)-phenylamine

https://huagongshe.com/reaction/1508092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-[2-(4-Nitrophenyl)ethyl]morpholineHCID 2797473—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-(2-morpholin-4-yl-ethyl)-phenylamineHCID 5899442758%

Reaction Steps

To a solution 4-[2-(4-nitro-phenyl)-ethyl]-morpholine (0.70 g, 2.97 mmol) (as prepared in the previous step) in 15 mL of MeOH was added 10% Pd/C (30 mg) and the mixture hydrogenated under 20 psi of H2 for 2 h. The mixture was filtered though Celite and concentrated. The residue was dissolved in DCM (20 mL) and NBS (0.53 g, 2.97 mmol) was added and the reaction stirred for 20 min at RT. The reaction was diluted with DCM (20 mL) and washed with NaHCO3 (2×40 mL) and the organic layer dried over Na2SO4 and concentrated. The title compound was eluted from a 20-g SPE with 100% EtOAc to give 0.49 g (58%) of a light yellow oil. Mass spectrum (ESI, m/z): Calcd. for C12H17BrN2O, 285.0 (M+H). found 285.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221797B2
Source datasetuspto-grants-2015_12
ORD IDord-b31ea82dad0d4dab8f5062a08d7d45bc
Source noteuspto-grants-2015_12