HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649830Generated: October 25, 2026
Hydrochloric Acid → 5-Amino-2-methoxybenzotrifluoride
https://huagongshe.com/reaction/649830
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitro-2-(trifluoromethyl)anisole | HCID 69562 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Amino-2-methoxybenzotrifluoride | HCID 600705 | — |
Reaction Steps
A suspension of 4-methoxy-3-trifluoromethyl-nitrobenzene (2.2 g) and iron powder (1.68 g) in ethanol (35 mL) and water (15 mL) is treated with a solution of concentrated hydrochloric acid (0.42 mL) in ethanol (6 mL) and water (3 mL) and the mixture is heated to reflux for approximately 1 hour. The mixture is then cooled, filtered, and concentrated under reduced pressure. The resulting oil is dissolved in ethyl acetate and extracted three times with 5% aqueous hydrochloric acid. The pooled acidic extracts are then cooled in an ice bath and basified with solid potassium carbonate, then extracted with ethyl acetate. These organic extracts are washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, concentrated under reduced pressure, then passed through a short column of silica gel (ethyl acetate is used as the eluant) to provide the desired compound as an amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271236B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-4d1a94bb82564ed5bd47bbf9850f6094 |
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| Source note | uspto-grants-2001_08 |
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