HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858020Generated: November 1, 2026
4-Nitro-3-phenethylaminobenzonitrile → 4-Amino-3-phenethylaminobenzonitrile
https://huagongshe.com/reaction/1858020
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitro-3-phenethylaminobenzonitrile | HCID 22125499 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4-Amino-3-phenethylaminobenzonitrile | HCID 22125554 | 100% |
Reaction Steps
A mixture comprising 3-methoxy-4-nitrobenzonitrile (1 g, 5.6 mmol), phenethylamine hydrochloride (1.8 g, 11.2 mmol), 50% sodium hydroxide (0.9 g, 11.2 mmol) and DMSO (3 mL) was heated at 100° C. for 3.5 hours, cooled and poured into a solution of 1N hydrochloric acid (200 mL, 0° C.). The mixture was stirred for 20 minutes to give a precipitate. The precipitate was collected and recrystallized from hot ethanol to provide 4-nitro-3-phenethylaminobenzonitrile (0.78 g, 2.9 mmol) as orange crystals. MS (CI), Calculated for C15H13N3O2, 267.3, Found (MH+): 282. A mixture comprising 4-nitro-3-phenethylaminobenzonitrile (0.75 g, 2.8 mmol), palladium on carbon (100 mg) and 1:1 methanol/THF (100 mL) was hydrogenated under 1 atm for 3 hours, filtered and concentrated under reduced pressure to provide 4-amino-3-phenethylaminobenzonitrile (0.68 g, 2.8 mmol) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150379 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-30d747610aec4362b4fc0082bda1358a |
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| Source note | uspto-grants-2000_11 |
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