HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446882Generated: October 31, 2026
2-Nitro-4-(trifluoromethyl)phenol → 2-Amino-4-(trifluoromethyl)phenol
https://huagongshe.com/reaction/1446882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitro-4-(trifluoromethyl)phenol | HCID 9816 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-(trifluoromethyl)phenol | HCID 120246 | 39.9% |
Reaction Steps
Sodium dithionite (97.0 g, 0.5 mole) was added in portions over a period of 6 hours to a solution of 2-nitro-4-trifluoromethylphenol (31 g, 0.15 mole) in a mixture of ethanol (120 ml) and water (90 ml), the solution being heated, with stirring, at a temperature of 55° C. during the addition. The mixture was filtered, the filtrate retained, and the collected solid was triturated with ethanol and refiltered. The solvent was removed from the combined filtrates by distillation under reduced pressure to give a yellow solid. The solid was dissolved in water, the aqueous solution extracted with diethyl ether (4×100 ml) and the combined ethereal phases were washed with brine. The ethereal phase was dried over anhydrous magnesium sulfate and the solvent evaporated to give a yellow solid which was recrystallised from petroleum ether (700 ml, bp 100°-120° C.) to give the title compound as a pale yellow solid (10.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04314065 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-6334f43f584f463aa5a189d3bf5ff654 |
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| Source note | uspto-grants-1982_02 |
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