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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048993Generated: October 30, 2026

N-bromobutanimide → 2-Bromo-5-(methylamino)-4-nitrobenzonitrile

https://huagongshe.com/reaction/1048993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant64910-48-1HCID 11019398—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAzobisisobutyronitrileHCID 6547—
Product2-Bromo-5-(methylamino)-4-nitrobenzonitrileHCID 66684862—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 3-(methylamino)-4-nitrobenzonitrile (0.9 g, 0.005 mol) and NBS (0.9 g, 0.005 mol) in DMF (15 ml), AIBN (catalytic) was carefully added and the resulting solution was stirred at 80° C. for 3 h. The reaction was diluted with H2O and extracted with dichloromethane (3×30 ml). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under vacuum to afford the title compound 2-bromo-5-(methylamino)-4-nitrobenzonitrile as a yellow solid. 1H NMR (400 MHz, CDCl3), δ: 8.44 (s, 1H), 8.04 (bs, 1H), 7.18 (s, 1H), 3.05 (s, 3H). MS (M+1): 256.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382226B2
Source datasetuspto-grants-2016_07
ORD IDord-a1919bef5a5a48e0aa61456ed993d6e2
Source noteuspto-grants-2016_07