HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Anilino-2-(4-fluoroanilino)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-anilino-2-(4-fluoroanilino)benzoate | HCID 57667985 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Anilino-2-(4-fluoroanilino)benzoic acid | HCID 57668077 | 100.2% |
Reaction Steps
To a suspension of ethanol 2.0 mL of methyl 4-anilino-2-(4-fluoroanilino)benzoate 0.25 g was added water 1.0 mL solution of sodium hydroxide 0.060 g at room temperature, and it was heated and refluxed for 2 hours. After the reaction mixture was cooled to room temperature,1.0 mol/L hydrochloric acid and ethyl acetate were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Diisopropyl ether and hexane were added to the obtained residue, and solid matter was filtrated to give 4-anilino-2-(4-fluoroanilino)benzoic acid 0.24 g of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08327467B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-83161d65338d4f10b63cd3c24e2270de |
| Source note | uspto-grants-2012_12 |