HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203652Generated: October 31, 2026
Ammonium Chloride → 3-(Trifluoromethoxy)pyridin-2-amine
https://huagongshe.com/reaction/2203652
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 19034689 | HCID 19034689 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Trifluoromethoxy)pyridin-2-amine | HCID 49871186 | — |
Reaction Steps
To a stirred solution of 2-nitro-3-(trifluoromethoxy)pyridine (370 mg, 1.78 mmol) in ethanol (5 mL) were added aqueous ammonium chloride (951 mg, 17.78 mmol, in 10 mL of water) and iron powder (993 mg, 17.78 mmol). The reaction mixture was heated to 70° C. for 2 h. After cooling down the reaction mixture was filtered and the solid was washed with ethyl acetate. The mother liquid was concentrated to dryness in vacuo. The residue was diluted with water and extracted with ethyl acetate (3×15 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was used in next step directly without further purification (250 mg, 79%): 1H NMR (400 MHz, DMSO-d6) δ 7.93-7.91 (m, 1H), 7.48-7.46 (m, 1H), 6.59-6.56 (m, 1H), 6.35 (brs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365583B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-96f4d3aae38045bf9bb9b737d394ae85 |
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| Source note | uspto-grants-2016_06 |
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