HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884963Generated: October 27, 2026
Acetic Acid → 2-Amino-5-chloro-4-(trifluoromethyl)phenol
https://huagongshe.com/reaction/884963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Chloro-2-nitro-4-(trifluoromethyl)phenol | HCID 10776504 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-chloro-4-(trifluoromethyl)phenol | HCID 14011736 | 81.7% |
Reaction Steps
A mixture of 7.55 g of 5-chloro-2-nitro-4-trifluoromethylphenol and 10 ml of ethyl acetate was added dropwise to a mixture, which was heated to 80° C., of 8.7 g of electrolytic iron, 30 ml of acetic acid and 50 ml of water, and then the reaction mixture was stirred at the same temperature for 30 minutes. The mixture was cooled to room temperature, and then water was added, followed by extraction with ethyl acetate. The combined organic layers were washed with water, a saturated aqueous solution of sodium hydrogencarbonate and a saturated sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 5.4 g of 2-amino-5-chloro-4-trifluoromethylphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242133B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-b0a00884c8864bc6aeb8206ce50eb34b |
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| Source note | uspto-grants-2012_08 |
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