HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 4-(acetylamino)-N-(4-hydroxyphenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | p-Acetamidobenzoic acid | HCID 19266 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(acetylamino)-N-(4-hydroxyphenyl)benzamide | HCID 869595 | — |
Reaction Steps
A solution of p-acetamidobenzoic acid (12.5 g.) in 250 ml. of tetrahydrofuran is treated with triethylamine (11.1 ml.). The mixture is then treated with isobutylchloroformate (10.4 ml.) and, after 5 min. at about 25° C., with p-aminophenol (13.3 g.) in 80 ml. of dry pyridine. After 40 min. the crude product is obtained by addition of 2 liters of water. The product is recrystallized from 500 ml. of hot methanol by dilution with 300 ml. of water as white crystals, 5.9 g., m.p. 275.0°-277.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010172 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-293fe4c4febd491faf717d9bd6c6b30c |
| Source note | uspto-grants-1977_03 |