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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 64910-48-1 | HCID 11019398 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Azobisisobutyronitrile | HCID 6547 | — |
| Product | 2-Bromo-5-(methylamino)-4-nitrobenzonitrile | HCID 66684862 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382226B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a1919bef5a5a48e0aa61456ed993d6e2 |
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| Source note | uspto-grants-2016_07 |
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