HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Amino-4-chloro-3-trifluoromethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Chloro-2-nitro-3-(trifluoromethyl)phenol | HCID 58148239 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-chloro-3-trifluoromethylphenol | HCID 58148280 | 80% |
Reaction Steps
A mixture of 1.57 g of 4-chloro-2-nitro-3-trifluoromethylphenol and 5 ml of ethyl acetate was added dropwise to a mixture, which was heated to 80° C., of 1.8 g of electrolytic iron, 7 ml of acetic acid and 7 ml of water, which was stirred 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 1.1 g of 2-amino-4-chloro-3-trifluoromethylphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445522B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a1e1f0ee3caf40f7b52cdf8ac4188011 |
| Source note | uspto-grants-2013_05 |