HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409685Generated: October 29, 2026
Potassium Hydroxide → 2,4-Dichloro-5-methoxy-3-trifluoromethylaniline
https://huagongshe.com/reaction/409685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(2,4-dichloro-5-methoxy-3-trifluoromethyl-phenyl)-acetamide | HCID 86625462 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Dichloro-5-methoxy-3-trifluoromethylaniline | HCID 86625460 | — |
Reaction Steps
A 2 M solution of KOH in water (1.87 mL) is added to a solution of N-(2,4-dichloro-5-methoxy-3-trifluoromethyl-phenyl)-acetamide (104 mg, 0.344 mmol) in EtOH (3 mL). After stirring for 3.5 h at 80° C. followed by cooling to RT, the solvent is evaporated and the residue is taken up in EtOAc and a saturated aqueous solution of NaHCO3. The separated aqueous layer is extracted twice with EtOAc. The organic phases are washed with brine, dried (Na2SO4), filtered and concentrated, providing the title compound: ESI-MS: 258/260 [M-H]−1; tR=4.8 min (system 1); TLC: Rf=0.54 (EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759517B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-9835d3d4c3ae44199156f49ba2c6c50b |
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| Source note | uspto-grants-2014_06 |
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