HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 3,5-Dichloro-4-ethoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3,5-Dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl ester | HCID 54404293 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,5-Dichloro-4-ethoxyaniline | HCID 15270884 | — |
Reaction Steps
Trifluoroacetic acid (5 mL) is added to solid (3,5-dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl ester (0.97 g) and the mixture is stirred for approximately 45 minutes at room temperature. Water is then added, and the mixture is cooled in an ice bath and basified with solid potassium carbonate. The solution is extracted three times with ethyl acetate and the combined organic phases are washed with saturated aqueous sodium chloride then dried over anhydrous sodium sulfate. Concentration under reduced pressure and recrystallization from hexanes provides the desired product as a pale yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271236B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-3874d6991ac74584837a7f7848eea57e |
| Source note | uspto-grants-2001_08 |