HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505037Generated: October 30, 2026
2-(2-chloro-5-nitrophenyl)-5-phenyl-1H-imidazole → 4-Chloro-3-(5-phenyl-1H-imidazol-2-yl) aniline
https://huagongshe.com/reaction/1505037
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(2-chloro-5-nitrophenyl)-5-phenyl-1H-imidazole | HCID 58006520 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Chloro-3-(5-phenyl-1H-imidazol-2-yl) aniline | HCID 49840820 | — |
Reaction Steps
To a solution of 2-(2-chloro-5-nitrophenyl)-5-phenyl-1H-imidazole (27 g, 90.3 mmol) in EtOH (200 ml) is added 5 nCl2.2H2O (71 g, 316 mmol). The mixture is refluxed for 2 hours, cooled to room temperature and then concentrated. Ethyl acetate (200 ml) and NaOH (25 g in 100 ml water) are added to the residue and the mixture is stirred for 10 minutes at room temperature. The solid is removed by filtering through celite pad. The filtrate is separated and the organic layer is further washed with brine, dried over anhydrous MgSO4 and concentrated. The crude product is purified by silica gel flash chromatography, eluted with 40% ethyl acetate in dichloromethane to afford 4-Chloro-3-(5-phenyl-1H-imidazol-2-yl) aniline as a brown solid. LC-MS m/z: 270.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216964B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-0a9e2c336d86421f92c5cdeac8cd5c0c |
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| Source note | uspto-grants-2015_12 |
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