HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853457Generated: October 31, 2026
Ethanol → 4-(4-Aminophenoxy)-2-butyrylaminopyridine
https://huagongshe.com/reaction/853457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Butyroylamino-4-(4-nitrophenoxy)pyridine | HCID 22936677 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Aminophenoxy)-2-butyrylaminopyridine | HCID 22936463 | — |
Reaction Steps
A mixture of 0.6 g of 2-butyrylamino-4-(4-nitrophenoxy)pyridine, 1.2 g of iron powder, 2.8 g of ammonium chloride, 10 ml of ethanol, 10 ml of dimethylformamide and 5 ml of water was vigorously stirred at 100° C. for 10 minutes. The reaction was filtered with celite, the solvent was distilled off under reduced pressure, and then water was added to the filtrate and extraction was performed with ethyl acetate. The extract was dried over magnesium sulfate and the solvent distilled off under reduced pressure to obtain 0.6 g of the target substance as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253286B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-81c4b0451e684897b689d131f1f3eb35 |
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| Source note | uspto-grants-2007_08 |
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