HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352261Generated: October 30, 2026
Hydrochloric Acid → 2,3,5,6-Tetrafluoro-4-methoxyaniline
https://huagongshe.com/reaction/352261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2,4,5-Tetrafluoro-3-methoxy-6-nitrobenzene | HCID 4261372 | — |
| Reactant | Tin atom | HCID 5352426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,5,6-Tetrafluoro-4-methoxyaniline | HCID 12566452 | 28% |
Reaction Steps
Then, 25 g of the 2,3,5,6-tetrafluoro-4-methoxynitrobenzene was added to a dispersion of 30.3 g of tin dispersed in 230 ml of 95% ethanol. Thereto was dropwise added 70 ml of concentrated hydrochloric acid with ice-cooling. The mixture was refluxed for 2 hours with heating. Then, the reaction mixture was poured into 1,000 ml of water. Thereto was added an aqueous sodium hydroxide solution until the water layer became alkaline. The organic layer was extracted with 500 ml of ether. The ether layer was washed with an aqueous sodium chloride solution and dried over MgSO4. The resulting solution was subjected to vacuum distillation to remove the ether. The residue was subjected to recrystallization from ligroin to obtain 6 g of 2,3,5,6-tetrafluoro-4-methoxyaniline (yield: 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06746722B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-abcb5bf680114cfa9d8dbb1f4a72d460 |
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| Source note | uspto-grants-2004_06 |
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