HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484536Generated: October 25, 2026
Butanamide, N-(3-nitrophenyl)- → N-(3-aminophenyl)butanamide
https://huagongshe.com/reaction/1484536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanamide, N-(3-nitrophenyl)- | HCID 346258 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-aminophenyl)butanamide | HCID 721132 | — |
Reaction Steps
A solution of N-(3-nitrophenyl)butyramide (8.60 g, 41.3 mmol) in MeOH (207 mL) was divided between two 500 mL flasks with stir bars. Each flask was flushed well with nitrogen, then 5% palladium on carbon (4.40 g, 2.065 mmol) was added, half to each flask. A 3-way adapter with a large hydrogen-filled balloon was attached to each flask, and the reactions were evacuated and back-filled with hydrogen five times, while stirring vigorously. The reactions were then stirred for 16 h, then filtered through a funnel packed with Celite. The filter cake was washed with MeOH, and the filtrate was concentrated, redissolved with DCM, then purified by column chromatography (EtOAc/hexanes gradient) to yield a white solid after precipitating from hexanes (5.87 g, 80%). LRMS (ESI+) (M+H): 179.18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422262B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ab42e9e2b73b467ea7ee1bb02c5702d7 |
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| Source note | uspto-grants-2016_08 |
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